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[ CAS No. 10602-04-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 10602-04-7
Chemical Structure| 10602-04-7
Structure of 10602-04-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 10602-04-7 ]

CAS No. :10602-04-7 MDL No. :MFCD05664205
Formula : C9H8O Boiling Point : -
Linear Structure Formula :- InChI Key :QCZORVSTESPHCO-UHFFFAOYSA-N
M.W : 132.16 Pubchem ID :11170993
Synonyms :
Chemical Name :(4-Ethynylphenyl)methanol

Calculated chemistry of [ 10602-04-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.11
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.5
TPSA : 20.23 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.07 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.84
Log Po/w (XLOGP3) : 1.46
Log Po/w (WLOGP) : 1.09
Log Po/w (MLOGP) : 2.1
Log Po/w (SILICOS-IT) : 2.31
Consensus Log Po/w : 1.76

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.96
Solubility : 1.46 mg/ml ; 0.011 mol/l
Class : Very soluble
Log S (Ali) : -1.49
Solubility : 4.27 mg/ml ; 0.0323 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.27
Solubility : 0.703 mg/ml ; 0.00532 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.58

Safety of [ 10602-04-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H302-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 10602-04-7 ]

* 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 [ 10602-04-7 ]

[ 10602-04-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13195-50-1 ]
  • [ 10602-04-7 ]
  • C13H9NO3S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; copper(l) iodide; In N,N-dimethyl-formamide; at 20 - 60℃; for 2h; A solution of compound 59ii (200 mg, 0.96 mmol) and 59iii (127 mg, 0.96 mmol) in DMF (3 ml) was degassed thrice and PdCl2(dppf) (50 mg, 0.07 mmol) was added to it, EPO <DP n="135"/>followed by CuI (8.5 mg, 0.043 mmol) and TEA (0.27 ml, 1.92 mmol), at rt, under argon atmosphere and the reaction mixture was heated at 60 0C for two hours. The reaction mixture was diluted with EA, washed with brine, the organic layer separated, dried, and concentrated to yield a residue which was separated by column chromatography on silica gel employing as eluent EA\\Hex (0-70percent) to yield compound 5Si.
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