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[ CAS No. 22775-90-2 ] {[proInfo.proName]}

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Chemical Structure| 22775-90-2
Chemical Structure| 22775-90-2
Structure of 22775-90-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 22775-90-2 ]

CAS No. :22775-90-2 MDL No. :MFCD00614884
Formula : C10H8Cl2N2Ni Boiling Point : -
Linear Structure Formula :- InChI Key :NSWRSAFGHPRHGG-UHFFFAOYSA-L
M.W : 285.78 Pubchem ID :155293741
Synonyms :

Calculated chemistry of [ 22775-90-2 ]

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 59.17
TPSA : 9.86 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.51
Log Po/w (WLOGP) : -3.85
Log Po/w (MLOGP) : 1.49
Log Po/w (SILICOS-IT) : 0.72
Consensus Log Po/w : 0.37

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.42
Solubility : 0.011 mg/ml ; 0.0000384 mol/l
Class : Moderately soluble
Log S (Ali) : -3.4
Solubility : 0.114 mg/ml ; 0.000398 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.29
Solubility : 1.45 mg/ml ; 0.00508 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.72

Safety of [ 22775-90-2 ]

Signal Word:Danger Class:9
Precautionary Statements:P501-P273-P260-P270-P264-P280-P391-P314-P337+P313-P305+P351+P338-P301+P312+P330 UN#:3077
Hazard Statements:H302-H319-H372-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 22775-90-2 ]

* 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 [ 22775-90-2 ]

[ 22775-90-2 ] Synthesis Path-Downstream   1~48

  • 1
  • [ 12080-32-9 ]
  • [ 55425-72-4 ]
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  • 2
  • [ 12080-32-9 ]
  • [ 1295-35-8 ]
  • [ 111-78-4 ]
  • [ 22775-90-2 ]
  • [ 12130-66-4 ]
  • 3
  • [ 366-18-7 ]
  • nickel(II) chloride hexahydrate [ No CAS ]
  • [ 22775-90-2 ]
YieldReaction ConditionsOperation in experiment
In methanol; water; at 100.0℃; for 8.0h; Synthesis of [Ni(binol)(bpy)]CH3OH complex. Toa solution of NiCl26H2O (0.235 g, 1 mmol) in 10 mLof water was added 2,2′- bipyridine (0.154g, 1 mmol)in 10 mL of methanol dropwise with continuous stirring.The reaction was stirred at 100C under refl ux for8 h. To the mixture was added a solution of rac-H2binol(0.286 g, 1 mmol) and NaOH (0.08 g, 2 mmol) in 20 mLof water-alcohol (1 : 1 mixture) dropwise with continuousstirring. The reaction mixture was stirred at 50C for5 h. After cooling the yellow-brown colored solid formedwas fi ltered, fi rst washed with water-methanol (1 : 1 mixture)for several times, and then with ether and dried in avacuum. Analytically calculated for NiC31H24O3N2, %:yield 66, C 70.1, H 4.52, N 5.28. Found, %: C 69.98, H4.55, N 5.21. 13C NMR spectrum, 125 MHz DMSO-d6, δ,ppm: 79.5, 116.4, 119.9, 121.4, 124.1, 124.7, 125.2, 127.3127.7, 128.2, 129.1, 134.1, 136.6, 154.4, 160.8, 162.7.
  • 4
  • [ 22775-90-2 ]
  • [ 106-38-7 ]
  • NiCl((C5H4N)2)(CH3C6H4) [ No CAS ]
  • 5
  • [ 79268-77-2 ]
  • [ 22775-90-2 ]
  • [ 15218-76-5 ]
  • 6
  • [ 79268-77-2 ]
  • [ 107-13-1 ]
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  • [ 35025-05-9 ]
  • [ 74-85-1 ]
  • [ 106-97-8 ]
  • 7
  • [ 366-18-7 ]
  • [ 22775-90-2 ]
  • [ 7681-11-0 ]
  • Ni(bip)2(H2O)2I2 [ No CAS ]
  • 9
  • [ 15218-76-5 ]
  • [ 507-20-0 ]
  • [ 22775-90-2 ]
  • [ 74-84-0 ]
  • [ 75-28-5 ]
  • [ 115-11-7 ]
  • [ 106-97-8 ]
  • 11
  • [ 22775-90-2 ]
  • [ 53356-73-3 ]
  • [Ni(2,2'-bipyridine)(P2(2,4,6-triisopropylphenyl)2))] [ No CAS ]
  • 12
  • [ 108-86-1 ]
  • [ 22775-90-2 ]
  • C6H5Ni(bpy)Cl [ No CAS ]
  • 13
  • [ 22775-90-2 ]
  • [ 644-97-3 ]
  • [Ni(2,2'-bipyridine)(P2Ph2))] [ No CAS ]
  • 14
  • [ 366-18-7 ]
  • [ 22775-90-2 ]
  • [ 15186-68-2 ]
  • 15
  • [ 366-18-7 ]
  • nickel dichloride [ No CAS ]
  • [ 22775-90-2 ]
YieldReaction ConditionsOperation in experiment
81.93% In ethanol; General procedure: The complexes, Cu(Bipy)Cl2,Ni(Bipy)Cl2, Co(Bipy)Cl2 were prepared by mixing one equivalent of 2,2′-bipyridine in 30 mL of ethanol to one equivalent of respective metal chlorides in 15 mL of ethanol.
  • 16
  • Ni(2,2'-bipyridyl)3Cl2 [ No CAS ]
  • [ 22775-90-2 ]
  • Ni(bip)2Cl2 [ No CAS ]
  • Ni(bip)1.33Cl2 [ No CAS ]
  • 17
  • [ 12107-56-1 ]
  • [ 55425-72-4 ]
  • [ 111-78-4 ]
  • [ 57811-65-1 ]
  • [ 22775-90-2 ]
  • 18
  • [ 366-18-7 ]
  • [ 1295-35-8 ]
  • [ 12107-56-1 ]
  • [ 111-78-4 ]
  • [ 57811-65-1 ]
  • [ 22775-90-2 ]
  • 19
  • [ 366-18-7 ]
  • [ 1295-35-8 ]
  • [ 12145-47-0 ]
  • [ 111-78-4 ]
  • [ 57811-65-1 ]
  • [ 22775-90-2 ]
  • 20
  • [ 41114-50-5 ]
  • [ 22775-90-2 ]
  • 24
  • [ 22775-90-2 ]
  • (η-5C5H5)Ni(bipy) [ No CAS ]
  • 25
  • [ 22775-90-2 ]
  • [ 53053-73-9 ]
  • 2,3,5,6-bis(o-carborano)-1,1-α,α'-dipyridylnickelous-4,4-dimethylsilacyclohexane [ No CAS ]
  • 26
  • [ 22775-90-2 ]
  • [ 66080-22-6 ]
  • 2,2'-bipyridylbis(pentafluorophenyl)nickel(II) [ No CAS ]
  • 27
  • [ 22775-90-2 ]
  • [ 72728-58-6 ]
  • 2,2'-bipyridylbis(2,3,5,6-tetrafluorophenyl)nickel(II) [ No CAS ]
  • 28
  • [ 366-18-7 ]
  • {NiCl(CClCCl2)(P(C6H5)3)2} [ No CAS ]
  • [ 22775-90-2 ]
  • [ 89486-79-3 ]
  • 29
  • [ 79354-84-0 ]
  • [ 22775-90-2 ]
  • [ 802294-64-0 ]
  • 31
  • [ 22775-90-2 ]
  • [ 141-52-6 ]
  • [ 119327-18-3 ]
  • [ 436154-27-7 ]
  • 32
  • [ 366-18-7 ]
  • [ 1295-35-8 ]
  • [ 90-13-1 ]
  • [ 22775-90-2 ]
  • [ 466645-96-5 ]
  • 33
  • [ 7647-01-0 ]
  • [ 225530-75-6 ]
  • [ 22775-90-2 ]
  • 34
  • [ 22775-90-2 ]
  • [ 105858-66-0 ]
  • [ 177279-27-5 ]
  • 35
  • [ 22775-90-2 ]
  • [ 576-83-0 ]
  • [ 104049-88-9 ]
  • 36
  • [ 22775-90-2 ]
  • [ 107658-48-0 ]
  • [ 685142-49-8 ]
  • 37
  • [ 12107-56-1 ]
  • [ 55425-72-4 ]
  • [ 111-78-4 ]
  • [ 22775-90-2 ]
  • [ 917346-04-4 ]
  • 38
  • [ 366-18-7 ]
  • [ 1295-35-8 ]
  • [ 12107-56-1 ]
  • [ 111-78-4 ]
  • [ 22775-90-2 ]
  • [ 917346-04-4 ]
  • 39
  • [ 498-66-8 ]
  • [ 12107-56-1 ]
  • [ 55425-72-4 ]
  • [ 22775-90-2 ]
  • [ 57205-95-5 ]
  • 40
  • [ 366-18-7 ]
  • nickel(II) dichloride hydrate [ No CAS ]
  • [ 22775-90-2 ]
  • 41
  • [ 22775-90-2 ]
  • [ 17148-97-9 ]
  • [ 1258938-68-9 ]
  • 42
  • [ 67-56-1 ]
  • [ 22775-90-2 ]
  • [ 602-09-5 ]
  • [Ni(1,1'-bi-2-naphtholate)(2,2-bipyridine)]*CH3OH [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In water; at 50.0℃; for 5.0h; Synthesis of [Ni(binol)(bpy)]CH3OH complex. Toa solution of NiCl26H2O (0.235 g, 1 mmol) in 10 mLof water was added 2,2′- bipyridine (0.154g, 1 mmol)in 10 mL of methanol dropwise with continuous stirring.The reaction was stirred at 100C under refl ux for8 h. To the mixture was added a solution of rac-H2binol(0.286 g, 1 mmol) and NaOH (0.08 g, 2 mmol) in 20 mLof water-alcohol (1 : 1 mixture) dropwise with continuousstirring. The reaction mixture was stirred at 50C for5 h. After cooling the yellow-brown colored solid formedwas fi ltered, fi rst washed with water-methanol (1 : 1 mixture)for several times, and then with ether and dried in avacuum. Analytically calculated for NiC31H24O3N2, %:yield 66, C 70.1, H 4.52, N 5.28. Found, %: C 69.98, H4.55, N 5.21. 13C NMR spectrum, 125 MHz DMSO-d6, δ,ppm: 79.5, 116.4, 119.9, 121.4, 124.1, 124.7, 125.2, 127.3127.7, 128.2, 129.1, 134.1, 136.6, 154.4, 160.8, 162.7.
  • 43
  • [ 22775-90-2 ]
  • [ 6117-80-2 ]
  • C14H15N2NiO2 [ No CAS ]
  • 44
  • [ 350-03-8 ]
  • [ 22775-90-2 ]
  • 45
  • [ 22775-90-2 ]
  • [ 100-51-6 ]
  • C17H15N2NiO [ No CAS ]
  • 46
  • [ 22775-90-2 ]
  • [ 5351-71-3 ]
  • [ 7732-18-5 ]
  • Ni(2,2'-bipyridine)(2-acetylthiophene thiosemicarbazone)*0.5H2O [ No CAS ]
YieldReaction ConditionsOperation in experiment
86.26% With sodium hydroxide; In ethanol; for 1.0h;Reflux; General procedure: A 1.2 g of ATT ligand (0.006 mol) was dissolved in 15 mL of 0.05 N NaOH in ethanol solvent in 100 mL beaker. A 1.0 g Cu(Bipy)Cl2 (0.003 mol) was dissolved in 15 mL of ethanol solvent in 100 mL beaker. Ligand solution and Cu(Bipy)Cl2 solution were transferred into 100 mL round bottom flask andheated under reflux for 1 h. On cooling the contents of flask,dark green coloured complex was formed. It was collected byfiltration, washed with small quantities of ethanol and driedin air. Ni(Bipy)ATT and Co(Bipy)ATT complexes are prepared similarly.
  • 47
  • [ 366-18-7 ]
  • nickel chloride monohydrate [ No CAS ]
  • [ 22775-90-2 ]
YieldReaction ConditionsOperation in experiment
88% In ethanol; for 4.5h;Reflux; Dissolve 1.48g of nickel chloride monohydrate in 25ml of ethanol with a mass concentration of 95%, place in a flask, heat to reflux, and dissolve 1.56g of 2,2'-bipyridine in 20ml of ethanol with a mass concentration of 95%, and add it with a dropping funnel For the above nickel chloride solution, the dropping time is controlled to 1.5h, and the reflux reaction is continued for 4h. The reaction mixture was cooled to room temperature and concentrated to 20ml. The solid that appeared was collected by filtration.And recrystallized in ethanol to obtain 2.51 g of precursor Ni(bpy)Cl2, with a yield of 88%.
  • 48
  • [ 22775-90-2 ]
  • C20H18N4 [ No CAS ]
  • C40H34Cl4N8Ni2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
In ethanol; dichloromethane; at 50.0℃; for 10.0h; Dissolve 1.48g of nickel chloride monohydrate in 25ml of ethanol with a mass concentration of 95%, place in a flask, heat to reflux, and dissolve 1.56g of 2,2'-bipyridine in 20ml of ethanol with a mass concentration of 95%, and add it with a dropping funnel For the above nickel chloride solution, the dropping time is controlled to 1.5h, and the reflux reaction is continued for 4h. The reaction mixture was cooled to room temperature and concentrated to 20ml. The solid that appeared was collected by filtration.And recrystallized in ethanol to obtain 2.51 g of precursor Ni(bpy)Cl2, with a yield of 88%.Put 0.858g (3mmol) of Ni(bpy)Cl2 in a two-necked flask, add 50ml of absolute ethanol; dissolve the aforementioned ligand L0.377g (1.2mmol) in 20ml of dichloromethane, and add dropwise to the flask with a dropping funnel. Control the dripping time for 2h,Heat to 50C and stir for 8 hours, concentrate on a rotary evaporator to about 25ml, filter, wash with cold ethanol, and dry in the air. Recrystallize in ethanol/water mixed solution to obtain binuclear nickel complex [Ni(bpy)]2LCl4 (as shown in the structure of formula I, M is a nickel atom).
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