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[ CAS No. 870-08-6 ] {[proInfo.proName]}

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Chemical Structure| 870-08-6
Chemical Structure| 870-08-6
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Product Details of [ 870-08-6 ]

CAS No. :870-08-6 MDL No. :MFCD00013839
Formula : C16H34OSn Boiling Point : -
Linear Structure Formula :- InChI Key :LQRUPWUPINJLMU-UHFFFAOYSA-N
M.W : 361.15 Pubchem ID :93563
Synonyms :

Calculated chemistry of [ 870-08-6 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 14
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 85.47
TPSA : 17.07 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -3.21 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 7.46
Log Po/w (WLOGP) : 6.13
Log Po/w (MLOGP) : 4.31
Log Po/w (SILICOS-IT) : 5.27
Consensus Log Po/w : 4.63

Druglikeness

Lipinski : 1.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -5.85
Solubility : 0.000504 mg/ml ; 0.0000014 mol/l
Class : Moderately soluble
Log S (Ali) : -7.65
Solubility : 0.00000807 mg/ml ; 0.0000000223 mol/l
Class : Poorly soluble
Log S (SILICOS-IT) : -6.59
Solubility : 0.0000926 mg/ml ; 0.000000256 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 3.0
Synthetic accessibility : 4.91

Safety of [ 870-08-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P302+P352-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 870-08-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 870-08-6 ]

[ 870-08-6 ] Synthesis Path-Downstream   1~85

YieldReaction ConditionsOperation in experiment
EXAMPLE 4 EQU35 It was prepared by the same method and using the same quantities as in Experiment 3 (except using dioctyltin oxide (0.05M) instead of dibutyltin oxide)
Compounds of the general formula: STR6 Dibutyltin dichloride; Dibutyltin dibromide; Dibutyltin oxide; Dibutyltin dilaurate; ... Tributyltin acetate; Tributyltin ethoxide; Triethyltin ethoxide; Triethyltin acetate; Dioctyltin oxide; Tributyltin chloride; Tributyltin trichloroacetate.
  • 3
  • [ 870-08-6 ]
  • [ 71-36-3 ]
  • [ 819792-07-9 ]
  • [ 32916-97-5 ]
YieldReaction ConditionsOperation in experiment
at 113℃; for 12h;Heating / reflux; Using a device as shown in Fig. 3, dioctyltin dialkoxides were produced as follows. Into a 5-liter SUS reaction vessel 1 equipped with a stirrer, a heater and a baffle were charged 108 g (0.3 mol) of dioctyltin oxide and 2,223 g (30 mol) of 1-butanol (manufactured and sold by Aldrich, U.S.A.), wherein dioctyltin oxide was fed through conduit 4 provided at the top of reaction vessel 1, and 1-butanol was fed from alcohol reservoir 16 through conduit 3 provided at an upper portion of reaction vessel 1. Further, nitrogen gas was fed to reaction vessel 1 through a SUS tube connected to inert gas conduit 2 provided at a lower portion of reaction vessel 1 at a rate of 0.5 N/hr. Subsequently, the contents of reaction vessel 1 were heated while stirring, so as to adjust the temperature thereof within the range of from 113 C to the boiling point of 1-butanol, thereby performing a reaction for about 12 hours while discharging low boiling point components in the form of a gas through gas discharging conduit 5 provided at an upper portion of reaction vessel 1. During the reaction, the gas discharged from conduit 5 was transferred through condenser 6 to reservoir 7 in which a liquid mixture containing 1-butanol and water was obtained. After the reaction, the resultant liquid reaction mixture in reaction vessel 1 was withdrawn from withdrawal conduit 8 and transferred to reservoir 9. From reservoir 9, the liquid reaction mixture was transferred through conduit 10 to apparatus 11 for removing alcohol, which was equipped with a stirrer, a pressure-reduction device and a heater. The above-mentioned operation was repeated two times (i.e., the above-mentioned operation was performed three times in total). Then, the liquid reaction mixture collected in apparatus 11 for removing alcohol was heated under reduced pressure to thereby gasify the unreacted alcohol contained in the liquid reaction mixture. The gasified alcohol was discharged from conduit 21, and transferred through condenser 6 to reservoir 16. The residual liquid having the alcohol removed therefrom was discharged from apparatus 11 and transferred through conduit 12 to reservoir 23. The liquid obtained in reservoir 23 was analyzed. As a result, it was found that the weight of the liquid was about 375 g, and that the liquid contained about 0.50 mol of dioctyltin dibutoxide and about 0.20 mol of 1,1,3,3-tetraoctyl-1,3-dibutyloxydistannoxane.
  • 4
  • Methyl 3-(5-phenylsulfonylbenzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydro-cinnamate [ No CAS ]
  • [ 2403-89-6 ]
  • [ 870-08-6 ]
  • [ 1027092-45-0 ]
YieldReaction ConditionsOperation in experiment
70% EXAMPLE 12 1,2,2,6,6-Pentamethylpiperidin-4-yl 3-(5-Phenylsulfonylbenzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate Methyl 3-(5-phenylsulfonylbenzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydro-cinnamate (5 g, 0.01 mol), xylenes (18 g, 0.17 mol), 1,2,2,6,6-pentamethyl-4-hydroxy-piperidine (2.1 g, 0.012 mol) and dioctyltin oxide (0.5 g, 0.0014 mol) are charged to a reactor and heated to 160 C. while being vigorously stirred. At the end of six hours, any remaining xylene is removed by distillation under vacuum. The crude yellow oil obtained is chromatographed through a pad of silica gel using ethyl aetate as the eluent. The title compound is obtained in a 70% yield as a low melting yellow solid, melting at 45-52 C., whose structure is consistent with 1Hnmr and mass spectrometry.
  • 5
  • [ 870-08-6 ]
  • [ 110-16-7 ]
  • dioctyltin maleate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 6b Preparation of dioctyltin maleate from maleic acid Maleic acid and dioctyltin oxide are added to a screw drier in accordance with Example 4b. At the exit, dioctyltin maleate (compound 4) is obtained as a white free-flowing powder.
  • 6
  • [ 108-31-6 ]
  • [ 870-08-6 ]
  • dioctyltin maleate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 5a Preparation of dioctyltin maleate from maleic anhydride Maleic anhydride and dioctyltin oxide are mixed with one another, and the mixture is reacted in a twin-screw laboratory extruder in accordance with Example 1. Dioctyltin maleate (compound 4) is obtained as the end product in the form of a white free-flowing powder.
EXAMPLE 5b Preparation of dioctyltin maleate from maleic anhydride Maleic anhydride and dioctyltin oxide are added to a screw drier in accordance with Example 4b. At the exit, dioctyltin maleate (compound 4) is obtained as a white free-flowing powder.
  • 7
  • [ 870-08-6 ]
  • [ 110-17-8 ]
  • dioctyltin fumarate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 2 Preparation of dioctyltin fumarate from fumaric acid A mixture of 6.03 kg of fumaric acid and 18.76 kg of dioctyltin oxide is heated in a batchwise operating kneading drier to 60 C. under a pressure of 120 hPa (=120 mbar) and dehydrated at constant pressure and temperature for 20 minutes. The product is then cooled to room temperature while thorough mixing is continued. This gives dioctyltin fumarate (compound 2) as a granular solid. Analysis C20 H36 O4 Sn: calc. 25.9% Sn; found 25.9% Sn; acid number (by titrimetry) 244.2 mg/g.
  • 8
  • [ 124-04-9 ]
  • [ 870-08-6 ]
  • dioctyltin adipate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 9 Preparation of dioctyltin adipate from adipic acid Adipic acid and dioctyltin oxide are introduced into a screw drier in accordance with Example 4b. At the exit, dioctyltin adipate (compound 6) is obtained as a white free-flowing powder.
  • 9
  • [ 870-08-6 ]
  • [ 88-99-3 ]
  • dioctyltin phthalate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 8 Preparation of dioctyltin phthalate from phthalic acid Phthalic acid and dioctyltin oxide are introduced into a screw drier in accordance with Example 4b. At the exit, dioctyltin phthalate (compound 5) is obtained as a white free-flowing powder.
  • 10
  • [ 111-20-6 ]
  • [ 870-08-6 ]
  • dioctyltin sebacate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 10 Preparation of dioctyltin sebacate from sebacic acid Sebacic acid and dioctyltin oxide are introduced into a screw drier in accordance with Example 4b. At the exit, dioctyltin sebacate (compound 7) is obtained as a white free-flowing powder.
  • 11
  • [ 870-08-6 ]
  • [ 107-96-0 ]
  • dioctyltin β-mercaptopropionate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 1 Preparation of Dioctyltin beta-mercaptopropionate In a kneading drier, 4.27 kg of beta-mercaptopropionic acid are added by spraying to 14.53 kg of dioctyltin oxide over a period of 6 minutes. The mixture thus obtained is heated at 60 C. for a period of 20 minutes with thorough mixing and under a pressure of 120 hPa (=120 mbar), during which the water of reaction formed escapes. The mixture is then cooled to room temperature while thorough mixing of the product is continued. Dioctyltin beta-mercaptopropionate is obtained as a white free-flowing solid. Analysis C19 H38 O3 S Sn: calc. 6.9 % S, 25.5 % Sn; found 6.0 % S, 25.3 % Sn; IR vibration at 1531 cm-1; chemical shift in 119 Sn NMR at +94 ppm.
  • 12
  • 2-ethylhexyl thiosalicylate [ No CAS ]
  • [ 870-08-6 ]
  • di-n-octyltin bis-[2-(2-ethylhexyloxycarbonyl)-phenylmercaptide] [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 1 Preparation of di-n-octyltin bis-[2-(2-ethylhexyloxycarbonyl)-phenylmercaptide] A mixture of 41.6 g of dioctyltin oxide (99% content) and 61.4 g of 2-ethylhexyl thiosalicylate (99% content) is heated at 100 C. under a vacuum of 20 mbar for 45 minutes, and the water formed in the reaction is removed. Clarification by filtration is carried out when the reaction is complete. The reaction product is a yellow, oily liquid. Refractive index nD20: 1.5475
  • 13
  • [ 124589-92-0 ]
  • [ 870-08-6 ]
  • di-n-octyltin bis-[4-(2-ethylhexyloxycarbonyl)-phenylmercaptide] [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 5 Preparation of di-n-octyltin bis-[4-(2-ethylhexyloxycarbonyl)-phenylmercaptide] 41.6 g of dioctyltin oxide (99% content) are reacted, as described in Example 1, with 61.4 g of 2-ethylhexyl p-mercaptobenzoate (99% content).
  • 14
  • [ 41651-93-8 ]
  • [ 870-08-6 ]
  • di-n-octyltin bis-[3-(ethoxycarbonyl)phenyl-mercaptide] [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 6 Preparation of di-n-octyltin bis-[3-(ethoxycarbonyl)phenyl-mercaptide] 51.6 g of dioctyltin oxide (99% content) are reacted, as described in Example (1), with 51.7 g of ethyl m-mercaptobenzoate (99.5% content).
  • 15
  • [ 92-50-2 ]
  • [ 870-08-6 ]
  • [ 80-62-6 ]
  • [ 2997-87-7 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; toluene; Preparation 7 N-ethyl-N-2-methacryloyloxyethylaniline To a stirred solution of N-ethyl-N-2-hydroxyethyl-aniline (4.95g: 0.03 mol) in toluene (50ml) under air was added methylmethacrylate (19ml; 0.178 mol) dioctyltinoxide (1.15g) and 1% topanol 'O' (0.2 ml solution in CH2Cl2). The mixture was heated at reflux under a steady air flow for twelve hours then the contents cooled and evaporated under reduced pressure to give the crude product (8.97g >100%). This was purified by flash chromatography (silica/hexane/ethyl acetate gradient) to give the product as a colourless oil (6.89g; 98%). 1Hnmr (250MHz; CDCl3; TMS 1.3t (3H), 2.0s (3H), 3.5m (4.4t (2H), 5.6s (1H), 6.2s (1H), 6.7m (3H), 7.2m (2H) ir (liquid film) 2950, 1720, 1600, 1500, 1360, 1300, 1160 cmmin1 Analysis found C, 72.4; H, 8.3; N, 5.8 C14H19NO2 requires C, 72.1; H, 8.2; N, 6.0%
  • 16
  • [ 26738-80-7 ]
  • [ 870-08-6 ]
YieldReaction ConditionsOperation in experiment
96.0% Thereafter, the lowermost layer was treated in the same manner as in Example 6, giving 115.4 g (96.0% yield) of di-n-octyltin oxide. Analysis revealed that the tin content was 32.85%, the halogen content less than 60 ppm and the total content of tri- and mono-n-octyltin oxide 3,000 ppm.
  • 17
  • [ 870-08-6 ]
  • [ 71-36-3 ]
  • [ 819792-07-9 ]
YieldReaction ConditionsOperation in experiment
96% at 127℃; for 2.5h; Example 8 (Preparation of the starting material 1,1,3,3-tetraoctyl-1,3-di(butyloxy)-distannoxane) A 2-liter recovery flask was charged with 217 g (0.6 mol) of dioctyltin oxide (manufactured by Wako Pure chemical Industries Ltd., Japan, 95%) and 445 g (6 mol) of 1-butanol (manufactured by Wako Pure chemical Industries Ltd., Japan, special grade), whereby the flask contained the resulting white slurry mixture. The flask was attached to an evaporator (manufactured by Shibata Scientific Technology Ltd., R-144) connected to a thermoregulator-equipped oil bath (manufactured by Masuda Corporation, Japan, OBH-24). The oil bath temperature was set at 127C. The flask was immersed in the oil bath, and rotation of the evaporator was started. Rotation was continued for about 150 minutes while stirring and heating under atmospheric pressure with the evaporator purge valve open. The flask was then removed from the oil bath and allowed to cool. The flask yielded 437 g of a viscous reaction solution. Results of 119Sn, 1H and 13C-NMR analysis showed that, using dioctyltin oxide as a reference, the reaction solution contained a 96% yield of 1,1,3,3-tetraoctyl-1,3-di(butyloxy)-distannoxane, and did not contain any dioctyl-di(butyloxy)tin.(Obtaining dioctyltin dialkoxide using a column reactor) Dioctyltin alkoxide was produced in a column reactor 1 such as that illustrated in Fig. 2. A 15 mm inner diameter and 850 mm total length (750 mm effective length) tube reactor made from SUS 316, which was furnished with a supply line 4 and an extraction vent line 5 on a reactor upper portion 2, and a gas supply line 7 and an extraction line 6 on a reactor lower portion 3, was packed with Helipack No. 3 (manufactured by Tokyo Tokushu Kanaami K.K., Japan). The temperature of a lower flange portion of the tube reactor and the portion extending to about 60 mm from the flange was controlled using a heater set to 150, while the temperature from the heating device upper portion to the upper flange of the tube reactor was controlled using a heater set to 140. Carbon dioxide gas was fed from the gas supply line 7 at 80 mL/min, and a feed pump was used to start feeding the reaction solution obtained as described above (mixed solution consisting of the starting material 1,1,3,3-tetraoctyl-1,3-di(butyloxy)-distannoxane and the reactant 1-butanol) from the supply line 4 at 10 g/Hr. The holding time in the reactor was 37 minutes. The internal pressure of the reactor was measured at about 0.2 MPa-G using a pressure gauge. Low boiling point substances, including water, began to be extracted in gaseous form from the extraction vent line 5 and high boiling point components began to flow out from the extraction line 6. Continuous feeding and continuous extraction operation was continued in this state for 4 hours. Analysis of the liquid extracted from the extraction line 6 showed that, using dioctyltin oxide as a reference, the liquid contained a dioctyltin alkoxide consisting of about a 43% yield of dioctyldi(butyloxy)tin and 1,1,3,3-tetraoctyl-1,3-di(butyloxy)-distannoxane. Trioctyltinbutoxide had a yield of 0.1%. Upon cooling of the gas phase extracted from the vent line, a two-layer transparent liquid was obtained, in which moisture was present. The dehydration rate in the column reactor was 0.0017 mol/Hr, which was greater than the value 0.00025 mol/Hr calculated from expression (16).
  • 18
  • [ 870-08-6 ]
  • [ 142-73-4 ]
  • [ 123376-13-6 ]
  • 19
  • [ 4408-64-4 ]
  • [ 870-08-6 ]
  • [ 123376-15-8 ]
  • 20
  • N-(1,4-dimethylbutylidene)-bis-o-arsanilic acid [ No CAS ]
  • [ 870-08-6 ]
  • Sn(C8H17)2As(O)3C6H4NC(CH3)C2H4C(CH3)NC6H4As(O)3Sn(C8H17)2 [ No CAS ]
  • 21
  • [ 824-40-8 ]
  • [ 870-08-6 ]
  • di-n-octyl tin di-picolinate N-oxide [ No CAS ]
  • 22
  • [ 824-40-8 ]
  • [ 870-08-6 ]
  • {(n-octyl)2Sn(picolinato-N-oxide)}2O [ No CAS ]
  • 25
  • [ 98-98-6 ]
  • [ 870-08-6 ]
  • [ 136561-00-7 ]
  • 26
  • [ 98-98-6 ]
  • [ 870-08-6 ]
  • [ 136577-74-7 ]
  • 27
  • [ 59-67-6 ]
  • [ 870-08-6 ]
  • [ 138748-27-3 ]
  • 28
  • [ 59-67-6 ]
  • [ 870-08-6 ]
  • [ 138748-05-7 ]
  • 29
  • [ 2398-81-4 ]
  • [ 870-08-6 ]
  • (n-C8H17)2Sn(nicotinate N-oxide)2 [ No CAS ]
  • 30
  • [ 55509-36-9 ]
  • [ 870-08-6 ]
  • 2CH3(CH2)7(1-)*Sn(4+)*CH3(OH)CCHC(CH3)NC6H4AsO3(2-)={CH3(CH2)7}2Sn{CH3(OH)CCHC(CH3)NC6H4AsO3} [ No CAS ]
  • 31
  • [ 55135-34-7 ]
  • [ 870-08-6 ]
  • 2CH3(CH2)7(1-)*Sn(4+)*C2H5OC(O)CH2C(CH3)NC6H4AsO3(2-)={CH3(CH2)7}2Sn{C2H5OC(O)CH2C(CH3)NC6H4AsO3} [ No CAS ]
  • 32
  • [ 103-04-8 ]
  • [ 870-08-6 ]
  • [ 133415-78-8 ]
  • 33
  • [ 103-04-8 ]
  • [ 870-08-6 ]
  • {((CH3(CH2)7)2Sn(O2CCH2S(C6H5)))2O}2 [ No CAS ]
  • 34
  • [ 721-65-3 ]
  • [ 870-08-6 ]
  • (C8H17)2Sn(O2C(CH2C6H5)C(H)N(H)C(O)CH2Cl)2 [ No CAS ]
  • 35
  • [ 721-65-3 ]
  • [ 870-08-6 ]
  • ((C8H17)2Sn(O2C(CH2C6H5)C(H)N(H)C(O)CH2Cl))2O [ No CAS ]
  • 36
  • [ 870-08-6 ]
  • [ 5115-65-1 ]
  • [ 143578-80-7 ]
  • 37
  • [ 870-08-6 ]
  • [ 5115-65-1 ]
  • {{(CH3(CH2)7)2Sn(O2CCH(CH(CH3)2)C8H4NO2)}2O}2 [ No CAS ]
  • 38
  • [ 533-75-5 ]
  • [ 870-08-6 ]
  • (C8H17)2Sn(C7H5O2)2 [ No CAS ]
  • 39
  • [ 870-08-6 ]
  • 5-(phenyldiazenyl)-8-hydroxyquinoline [ No CAS ]
  • (C8H17)2Sn(C9H5N(O)N2C6H5)2 [ No CAS ]
  • 40
  • [ 870-08-6 ]
  • [ 21860-84-4 ]
  • (C8H4O2NCH(CH3)COO)2Sn(CH3CH2CH2CH2CH2CH2CH2CH2)2 [ No CAS ]
  • 41
  • [ 870-08-6 ]
  • [ 21860-84-4 ]
  • 2C8H4O2NCH(CH3)COO(1-)*4(CH2)7CH3(1-)*2Sn(4+)*O(2-)=((C8H4O2NCH(CH3)COO)Sn(CH3CH2CH2CH2CH2CH2CH2CH2)2)2O [ No CAS ]
  • 42
  • [ 826-81-3 ]
  • [ 870-08-6 ]
  • (C8H17)2Sn(C9NH5(CH3)O)2 [ No CAS ]
  • 43
  • N-(benzoyl)-N'-(ferrocenylidene)hydrazine [ No CAS ]
  • [ 870-08-6 ]
  • (C8H17)2Sn((C5H5)Fe(C5H4CHNNCOC6H5))2 [ No CAS ]
  • 44
  • formyl ferrocene-2-isonicotinoyl hydrazone [ No CAS ]
  • [ 870-08-6 ]
  • (C8H17)2Sn((C5H5)Fe(C5H4CHNNCOC5H4N))2 [ No CAS ]
  • 45
  • formylferrocenyl salicyloylhydrazone [ No CAS ]
  • [ 870-08-6 ]
  • (C8H17)2Sn((C5H5)Fe(C5H4CHNNCOC6H4OH))2 [ No CAS ]
  • 46
  • [ 870-08-6 ]
  • [ 5123-55-7 ]
  • 2C8H4O2NCH(CH2C6H5)COO(1-)*4(CH2)7CH3(1-)*2Sn(4+)*O(2-)=((C8H4O2NCH(CH2C6H5)COO)Sn(CH3CH2CH2CH2CH2CH2CH2CH2)2)2O [ No CAS ]
  • 47
  • [ 870-08-6 ]
  • [ 5123-55-7 ]
  • (C8H4O2NCH(CH2C6H5)COO)2Sn(CH3CH2CH2CH2CH2CH2CH2CH2)2*4H2O [ No CAS ]
  • 48
  • [ 55-22-1 ]
  • [ 870-08-6 ]
  • [ 139739-78-9 ]
  • 49
  • [ 55-22-1 ]
  • [ 870-08-6 ]
  • [ 139720-07-3 ]
  • 50
  • [ 870-08-6 ]
  • [ 2419-38-7 ]
  • ((C8H4O2NCH(CH2CH(CH3)2)COO)Sn(CH3CH2CH2CH2CH2CH2CH2CH2)2)2O [ No CAS ]
  • 51
  • [ 870-08-6 ]
  • [ 2419-38-7 ]
  • (C8H4O2NCH(CH2CH(CH3)2)COO)2Sn(CH2CH2CH2CH2CH2CH2CH2CH3)2*3H2O [ No CAS ]
  • 52
  • (C5H5)Fe(C5H4CHNNHCOC6H4NO2) [ No CAS ]
  • [ 870-08-6 ]
  • (C8H17)2Sn((C5H5)Fe(C5H4CHNNCOC6H4NO2))2 [ No CAS ]
  • 53
  • (C5H5)Fe(C5H4CHNNHCOC6H4Cl) [ No CAS ]
  • [ 870-08-6 ]
  • (C8H17)2Sn((C5H5)Fe(C5H4CHNNCOC6H4Cl))2 [ No CAS ]
  • 54
  • [ 13602-12-5 ]
  • [ 870-08-6 ]
  • [ 139720-14-2 ]
  • 55
  • [ 13602-12-5 ]
  • [ 870-08-6 ]
  • (C8H17)2Sn(C5H4NOCOO)2 [ No CAS ]
  • 56
  • [ 870-08-6 ]
  • [ 72599-81-6 ]
  • 2(C8H17)(1-)*Sn(4+)*(OCHOCHOCHOCH2)(3-)*H(1+)=(C8H17)2Sn(C4H6O4) [ No CAS ]
  • 57
  • [ 870-08-6 ]
  • [ 122-59-8 ]
  • (C8H17)2Sn(C6H5OCH2COO)2 [ No CAS ]
  • 58
  • [ 2018-61-3 ]
  • [ 870-08-6 ]
  • (C11H12NO3)2Sn(C8H17)2 [ No CAS ]
  • 59
  • [ 2018-61-3 ]
  • [ 870-08-6 ]
  • ((C11H12NO3)Sn(C8H17)2)2O [ No CAS ]
  • 60
  • [ 33407-10-2 ]
  • [ 870-08-6 ]
  • [ 109031-86-9 ]
  • 61
  • [ 33407-10-2 ]
  • [ 870-08-6 ]
  • [ 109031-90-5 ]
  • 63
  • [ 870-08-6 ]
  • [ 58-96-8 ]
  • Sn(4+)*2C8H17(1-)*C5H7O4(C4H3N2O2)(2-)=(C8H17)2Sn(C5H7O4(C4H3N2O2)) [ No CAS ]
  • 64
  • [ 870-08-6 ]
  • [ 120-46-7 ]
  • [ 84887-57-0 ]
  • 65
  • [ 870-08-6 ]
  • [ 58-61-7 ]
  • di-n-octyltin adenosinate [ No CAS ]
  • 66
  • [ 870-08-6 ]
  • [ 118-00-3 ]
  • Sn(4+)*2C8H17(1-)*C5H7O4(C5H4N5O)(2-)=(C8H17)2Sn(C5H7O4(C5H4N5O)) [ No CAS ]
  • 67
  • [ 3646-73-9 ]
  • [ 870-08-6 ]
  • 2(C8H17)(1-)*Sn(4+)*(OCCH2OOCHOCHOCHOCH2)(5-)*3H(1+)=(C8H17)2Sn(C6H10O6) [ No CAS ]
  • 68
  • [ 870-08-6 ]
  • [ 65-46-3 ]
  • Sn(4+)*2C8H17(1-)*C5H7O4(C4N2H2(NH2)O)(2-)=(C8H17)2Sn(C5H7O4(C4N2H2(NH2)O)) [ No CAS ]
  • 69
  • [ 1188-21-2 ]
  • [ 870-08-6 ]
  • (C8H14NO3Sn(C8H17)2)2O [ No CAS ]
  • 70
  • [ 1188-21-2 ]
  • [ 870-08-6 ]
  • (C8H14NO3)2Sn(C8H17)2 [ No CAS ]
  • 71
  • [ 870-08-6 ]
  • [ 634-97-9 ]
  • [(NHC4H3COO)Sn(C8H17)2]2O [ No CAS ]
  • 72
  • [ 870-08-6 ]
  • [ 634-97-9 ]
  • (NHC4H3COO)2Sn(C8H17)2 [ No CAS ]
  • 73
  • [ 98-05-5 ]
  • [ 870-08-6 ]
  • 2C8H17(1-)*Sn(4+)*O3AsC6H5(2-)=(C8H17)2Sn(O3AsC6H5) [ No CAS ]
  • 75
  • [ 65423-87-2 ]
  • [ 870-08-6 ]
  • Sn(4+)*2CH3(CH2)7(1-)*O3AsCH2CH2OH(2-)*2C2H5OH=(CH3(CH2)7)2Sn(O3AsCH2CH2OH)*2C2H5OH [ No CAS ]
  • 76
  • [ 620-27-9 ]
  • [ 870-08-6 ]
  • ((CH3(CH2)7)2SnO3AsCH2C6H5)2 [ No CAS ]
  • 77
  • [ 618-20-2 ]
  • [ 870-08-6 ]
  • 2C8H17(1-)*Sn(4+)*O3AsC6H4COOH(2-)=(C8H17)2Sn(O3AsC6H4COOH) [ No CAS ]
  • 78
  • [ 13911-63-2 ]
  • [ 870-08-6 ]
  • (CH3(CH2)7)2SnO2As(C6H5)CH2COO [ No CAS ]
  • 79
  • [ 55509-30-3 ]
  • [ 870-08-6 ]
  • Sn(C8H17)2(O3AsC6H4NCHC6H5)*2H2O [ No CAS ]
  • 80
  • [ 20717-68-4 ]
  • [ 870-08-6 ]
  • 2C8H17(1-)*Sn(4+)*(CH2As(C6H5)O2)2(2-)=(C8H17)2Sn(CH2As(C6H5)O2)2 [ No CAS ]
  • 82
  • [ 870-08-6 ]
  • [ 85429-62-5 ]
  • (S-benzyl-β-N-(2-hydroxy-5-chlorophenyl)methylenedithiocabazato)dioctyltin [ No CAS ]
  • 83
  • [ 870-08-6 ]
  • [ 85429-61-4 ]
  • (S-benzyl-β-N-(2-hydroxy-5-bromophenyl)methylenedithiocabazato)dioctyltin [ No CAS ]
  • 84
  • [ 1028-71-3 ]
  • [ 870-08-6 ]
  • bis(5-benzoyl-8-quinolinolato)dioctyltin(IV) [ No CAS ]
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