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[ CAS No. 699-02-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 699-02-5
Chemical Structure| 699-02-5
Structure of 699-02-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 699-02-5 ]

CAS No. :699-02-5 MDL No. :MFCD00002904
Formula : C9H12O Boiling Point : No data available
Linear Structure Formula :- InChI Key :DAVFJRVIVZOKKS-UHFFFAOYSA-N
M.W : 136.19 Pubchem ID :95294
Synonyms :

Calculated chemistry of [ 699-02-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 2
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.34
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) : -5.65 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.98
Log Po/w (XLOGP3) : 2.09
Log Po/w (WLOGP) : 1.53
Log Po/w (MLOGP) : 2.19
Log Po/w (SILICOS-IT) : 2.48
Consensus Log Po/w : 2.05

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.31
Solubility : 0.662 mg/ml ; 0.00486 mol/l
Class : Soluble
Log S (Ali) : -2.14
Solubility : 0.976 mg/ml ; 0.00716 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.99
Solubility : 0.14 mg/ml ; 0.00103 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 699-02-5 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 699-02-5 ]

* 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 [ 699-02-5 ]

[ 699-02-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 622-47-9 ]
  • [ 611-14-3 ]
  • [ 699-02-5 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; COMPARATIVE EXAMPLE 1 In the same manner as in Example 1 but not using triethylamine, the reaction was carried out to give the following results: conversion of p-methylphenylacetic acid, 99.2%; yield of p-methylphenethyl alcohol, 74.3%; selectivity to p-methylphenethyl alcohol, 74.9%; yield of ethyltoluene, 10.2%.
  • 2
  • dirhenium heptoxide [ No CAS ]
  • [ 622-47-9 ]
  • [ 611-14-3 ]
  • [ 699-02-5 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In 1,4-dioxane; EXAMPLE 1 Into a 50 ml volume stainless steel made autoclave equipped with a magnetic stirrer and inserted with a glass tube, p-methylphenylacetic acid (0.6 g), dehydrated dioxane (10 ml), dirhenium heptoxide (60 mg) and triethylamine (4.3 mg) were charged, and the inner atmosphere was replaced by nitrogen gas. Hydrogen gas was pressurized therein up to 100 atm. The reaction was carried out at 162 C. for 5 hours while stirring. After cooling to room temperature, the reaction mixture was subjected to gas chromatographic analysis to give the following results: conversion of p-methylphenylacetic acid, 98.5%; yield of p-methylphenethyl alcohol, 92.4%; selectivity to p-methylphenethyl alcohol, 93.8%; yield of ethyltoluene, 0.5%.
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