Home Cart 0 Sign in  

[ CAS No. 19814-75-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 19814-75-6
Chemical Structure| 19814-75-6
Structure of 19814-75-6 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 19814-75-6 ]

Related Doc. of [ 19814-75-6 ]

Alternatived Products of [ 19814-75-6 ]

Product Details of [ 19814-75-6 ]

CAS No. :19814-75-6 MDL No. :MFCD00134434
Formula : C15H14O Boiling Point : -
Linear Structure Formula :- InChI Key :MTVNAPYHLASOSX-UHFFFAOYSA-N
M.W : 210.27 Pubchem ID :606997
Synonyms :

Calculated chemistry of [ 19814-75-6 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.2
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 65.47
TPSA : 9.23 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.79
Log Po/w (XLOGP3) : 4.32
Log Po/w (WLOGP) : 4.12
Log Po/w (MLOGP) : 3.74
Log Po/w (SILICOS-IT) : 4.13
Consensus Log Po/w : 3.82

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.42
Solubility : 0.00799 mg/ml ; 0.000038 mol/l
Class : Moderately soluble
Log S (Ali) : -4.23
Solubility : 0.0124 mg/ml ; 0.0000592 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.7
Solubility : 0.000423 mg/ml ; 0.00000201 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.55

Safety of [ 19814-75-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280 UN#:N/A
Hazard Statements:H317 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 19814-75-6 ]

* 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.

  • Upstream synthesis route of [ 19814-75-6 ]
  • Downstream synthetic route of [ 19814-75-6 ]

[ 19814-75-6 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 90-47-1 ]
  • [ 75-24-1 ]
  • [ 19814-75-6 ]
Reference: [1] Journal of the American Chemical Society, 1990, vol. 112, # 24, p. 8902 - 8906
  • 2
  • [ 7073-69-0 ]
  • [ 108-95-2 ]
  • [ 19814-75-6 ]
Reference: [1] RSC Advances, 2016, vol. 6, # 25, p. 20588 - 20597
  • 3
  • [ 19814-75-6 ]
  • [ 1079-66-9 ]
  • [ 161265-03-8 ]
YieldReaction ConditionsOperation in experiment
88%
Stage #1: With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium In tert-butyl methyl ether; cyclohexane at 6 - 10℃;
Stage #2: at 20℃; for 14 h;
Stage #3: at 10 - 20℃; for 5.16667 h;
Example 2A
Preparation of 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene, Xantphos
To a 5L round bottom flask (RBF) are added MTBE (2.5 L), 9,9-dimethylxanthene (131.4 g, 0.60 mole) and TMEDA (155 g, 1.32 mole).
After degassing the solution, s-BuLi (1.11 L, 1.3 M in cyclohexane, 1.44 mole) is cannulated into a dropping funnel and then slowly added over 60 min while maintaining the batch temperature at 6-10° C.
The mixture is then aged for 14 h at room temperature.
Ph2PCl is added slowly via a dropping funnel while maintain the mildly exothermic reaction at 10-20° C.
~60percent of the Ph2PCl (175 mL, 0.93 mole) is added in 0.5 hour.
The mixture is aged for 10 minutes before addition of the remaining Ph2PCl (120 mL, 0.63 mole).
After aged for 5 h at room temperature, the reaction is quenched with MeOH (9.9 mL, 0.24 mole).
The product is filtered and the slightly yellow solid is washed consecutively with MTBE (250 mL), MeOH (2*250 mL), water (2*300 mL), MeOH (2*250 mL) and MTBE (250 mL) and dried to give an off-white solid as product (304.2 g, 88percent yield).
77%
Stage #1: With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium In tert-butyl methyl ether; cyclohexane at 10 - 20℃; for 16 h;
Stage #2: at 20℃; for 5.75 h;
Example 2
Preparation of 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene, Xantphos
To a 1L round bottom flask (RBF) are added MTBE (500 mL), 9,9-dimethylxanthene (26.65 g) and TMEDA (30.6 g).
After degassing the solution, s-BuLi (155 g, 1.3 M in cyclohexane) is cannulated into a dropping funnel and then slowly added over 30 min while maintaining the batch temperature at 10-20° C.
The mixture is then aged for 16 h at room temperature.
Ph2PCl is added slowly via a dropping funnel while maintain the mildly exothermic reaction at 10-20° C.
~60percent of the Ph2PCl (30 mL) is added in 0.5 hour.
The mixture is aged for 15 minutes before addition of the remaining Ph2PCl.
After aged for 5.5 h at room temperature, the reaction is quenched with MeOH (2.0 mL).
The product is filtered and the slightly yellow solid is washed consecutively with MeOH (200 mL), water (200 mL), MeOH (200 mL) and MTBE (200 mL) and dried to give an off-white solid as product (54.8 g, 77percent yield).
Reference: [1] Patent: US2004/23979, 2004, A1, . Location in patent: Page/Page column 9; 10
[2] Patent: US2004/23979, 2004, A1, . Location in patent: Page/Page column 9
[3] Dalton Transactions, 2018, vol. 47, # 11, p. 3745 - 3754
[4] Tetrahedron Letters, 1995, vol. 36, # 1, p. 75 - 78
[5] Patent: US7612241, 2009, B1, . Location in patent: Page/Page column 4-5
[6] Patent: US2004/23978, 2004, A1, . Location in patent: Page/Page column 15;16
[7] Patent: US2004/23981, 2004, A1, . Location in patent: Page/Page column 17
[8] Dyes and Pigments, 2012, vol. 94, # 3, p. 561 - 569
  • 4
  • [ 19814-75-6 ]
  • [ 161265-03-8 ]
Reference: [1] Patent: US2004/23980, 2004, A1, . Location in patent: Page/Page column 15
Same Skeleton Products
Historical Records