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Merck
CN

189944

环戊基苯乙酸

97%

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关于此项目

线性分子式:
C5H9CH(C6H5)CO2H
化学文摘社编号:
分子量:
204.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-454-3
MDL number:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

98-100 °C (lit.)

solubility

methanol: soluble 50 mg/mL, clear, colorless

functional group

carboxylic acid, phenyl

SMILES string

OC(=O)C(C1CCCC1)c2ccccc2

InChI

1S/C13H16O2/c14-13(15)12(11-8-4-5-9-11)10-6-2-1-3-7-10/h1-3,6-7,11-12H,4-5,8-9H2,(H,14,15)

InChI key

BCJIDGDYYYBNNB-UHFFFAOYSA-N

Application

Cyclopentylphenylacetic acid was used in the synthesis of:
  • 1-cyclopentyl-l-phenyl-2-(p-alkoxyphenyl)ethylenes
  • soft ester analogs of anticholinergics


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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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664. Chemical constitution and sex-hormonal activity: the synthesis of of some 1-cyclopentyl-and 1-cyclohexyl-1: 2-diarylethylenes.
Hey DH and Musgrave OC.
Journal of the Chemical Society, 3156-3164 (1949)
F Huang et al.
Die Pharmazie, 57(2), 115-121 (2002-03-07)
Four new soft anticholinergic agents based on tropyl alpha-phenylcyclopentylacetate, 15a, 15b, 18a, and 18b, were designed and synthesized. Receptor binding studies on the cloned human muscarinic receptors indicated that the new soft anticholinergic agents possessed moderate potency as pKi ranged
B Liebmann et al.
Arzneimittel-Forschung, 42(11), 1354-1358 (1992-11-01)
Ester hydrolysis represents an important biotransformation pathway for various parasympatholytic agents. Cleavage of the ciclotropium ester bond results in the formation of alpha-phenylciclopentylacetic acid (PCA). The relevance of this metabolic route for ciclotropium bromide (HIT-PCE, CAS 85166-20-7) including its stereochemical



全球贸易项目编号

货号GTIN
189944-5G04061831810028