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189944

Sigma-Aldrich

Cyclopentylphenylacetic acid

97%

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About This Item

Fórmula lineal:
C5H9CH(C6H5)CO2H
Número de CAS:
3900-93-4
Peso molecular:
204.26
EC Number:
223-454-3
MDL number:
MFCD00001379
UNSPSC Code:
12352100
PubChem Substance ID:
24851406
NACRES:
NA.22

assay

97%

form

solid

mp

98-100 °C (lit.)

solubility

methanol: soluble 50 mg/mL, clear, colorless

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

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Application

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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N Bodor et al.
Journal of medicinal chemistry, 23(5), 474-480 (1980-05-01)
A new class of antimuscarinic drugs was designed and synthesized. The compounds are "soft" quaternary ammonium esters in which there is only one carbon atom separating the ester oxygen and the quaternary head. The compounds are potent anticholinergics when derived
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
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)
Radoslaw Laufer et al.
Bioorganic & medicinal chemistry, 22(17), 4968-4997 (2014-07-22)
TTK kinase was identified by in-house siRNA screen and pursued as a tractable, novel target for cancer treatment. A screening campaign and systematic optimization, supported by computer modeling led to an indazole core with key sulfamoylphenyl and acetamido moieties at

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