Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

P22354

Sigma-Aldrich

trans-2-Phenylcyclopropane-1-carboxylic acid

95%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C6H5C3H4CO2H
CAS Number:
939-90-2
Molecular Weight:
162.19
Beilstein/REAXYS Number:
3197783
EC Number:
213-366-3
MDL number:
MFCD00001292
UNSPSC Code:
12352100
PubChem Substance ID:
24898295
NACRES:
NA.22

Quality Level

100

assay

95%

form

powder

mp

86-88 °C (lit.)

SMILES string

OC(=O)[C@@H]1C[C@H]1c2ccccc2

InChI

1S/C10H10O2/c11-10(12)9-6-8(9)7-4-2-1-3-5-7/h1-5,8-9H,6H2,(H,11,12)/t8-,9+/m0/s1

InChI key

AHDDRJBFJBDEPW-DTWKUNHWSA-N

Looking for similar products? Visit Product Comparison Guide

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)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

R E Gerkin
Acta crystallographica. Section C, Crystal structure communications, 53 ( Pt 12), 1989-1991 (1998-02-12)
The title compound, (+/-)-cis-2-phenylcyclopropanecarboxylic acid, C10H10O2, crystallized in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic dimer type about a center of symmetry; the Odonor...Oacceptor distance is 2.645 (2) A. The carboxylic H atom is ordered
R E Gerkin
Acta crystallographica. Section C, Crystal structure communications, 53 ( Pt 9), 1280-1282 (1997-10-06)
The title compound, C10H10O2, crystallized in space group P2(1) with two molecules in the asymmetric unit. In this structure, hydrogen bonding of the cyclic dimer type [with O ... O 2.623(2)-2.637(2)A] links the two molecules of the asymmetric unit. The
Edmund J Keliher et al.
Organic & biomolecular chemistry, 4(14), 2777-2784 (2006-07-11)
Many carbenoid cyclopropanation reactions promoted by chiral catalysts give product mixtures reflecting impressive diastereo- and enantioselectivities. Few provide a single chiral product efficiently. This limitation has been overcome in cyclopropanations of styrene and isotopically labeled styrenes with alpha-diazoacetates. Convenient syntheses

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service