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[ CAS No. 97364-15-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 97364-15-3
Chemical Structure| 97364-15-3
Structure of 97364-15-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 97364-15-3 ]

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Product Details of [ 97364-15-3 ]

CAS No. :97364-15-3 MDL No. :MFCD00870634
Formula : C9H10O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UBXQIJLWYJGCCO-UHFFFAOYSA-N
M.W : 166.17 Pubchem ID :506061
Synonyms :

Calculated chemistry of [ 97364-15-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 44.34
TPSA : 57.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.5
Log Po/w (XLOGP3) : 1.42
Log Po/w (WLOGP) : 1.11
Log Po/w (MLOGP) : 1.37
Log Po/w (SILICOS-IT) : 1.23
Consensus Log Po/w : 1.33

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.0
Solubility : 1.65 mg/ml ; 0.00993 mol/l
Class : Soluble
Log S (Ali) : -2.23
Solubility : 0.972 mg/ml ; 0.00585 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.62
Solubility : 3.95 mg/ml ; 0.0238 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.35

Safety of [ 97364-15-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 97364-15-3 ]

* 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 [ 97364-15-3 ]

[ 97364-15-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 84851-56-9 ]
  • [ 97364-15-3 ]
YieldReaction ConditionsOperation in experiment
To a solution of methyl-4-(l-hydroxyethyl)benzoate (2.00 g, 11.10 mmol) in a mixture of THF (20 mL) and MeOH (10 mL) was added 1 M KOH (13.32 mL, 13.32 mmol). After stirring at room temperature overnight, the solution was diluted with 2 N HCl and extracted with EtOAc (4x). The combined organic layers were dried (MgSO4) and evaporated to give 4-(l-hydroxyethyl)benzoic acid as a colorless solid. 1H NMR (DMSO-dzeta, 600 MHz) delta 7.86 (d, J = 8.6 Hz, 2H), 7.43 (d, J = 8.3 Hz, 2H), 4.75 (q, J = 6.5 Hz, IH), 1.30 (d, J = 6.6 Hz, 3H). MS: cal'd 167 (MH+), exp 167 (MH+).
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