Skip to Content
MilliporeSigma
All Photos(1)

Documents

130966

Sigma-Aldrich

α-Chlorophenylacetyl chloride

technical grade, 90%

Synonym(s):

α-Chloro-α-phenylacetyl chloride, α-Chlorobenzeneacetyl chloride, (±)-2-Chloro-2-phenylacetyl chloride, 2-Chloro-2-phenylacetyl chloride, 2-Phenyl-2-chloroacetyl chloride, Phenyl(chloro)acetyl chloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5CHClCOCl
CAS Number:
2912-62-1
Molecular Weight:
189.04
Beilstein/REAXYS Number:
1073019
EC Number:
220-826-7
MDL number:
MFCD00000857
UNSPSC Code:
12352100
PubChem Substance ID:
24847984
NACRES:
NA.22

grade

technical grade

Quality Level

100

assay

90%

form

liquid

refractive index

n20/D 1.544 (lit.)

bp

120 °C/23 mmHg (lit.)

density

1.196 g/mL at 25 °C (lit.)

SMILES string

ClC(C(Cl)=O)c1ccccc1

InChI

1S/C8H6Cl2O/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H

InChI key

FGEAOSXMQZWHIQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

α-Chlorophenylacetyl chloride was used in the synthesis of α-chlorophenylacetic acid (CPAA). It was also used to prepare chloro-telechelic macroinitiators.

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3 - Water-react 3

target_organs

Respiratory system

Storage Class

4.3 - Hazardous materials, which set free flammable gases upon contact with water

wgk_germany

WGK 3

flash_point_f

123.8 °F

flash_point_c

51 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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

Customers Also Viewed

Slide 1 of 1

1 of 1

α-Bromoisobutyryl bromide 98%

Sigma-Aldrich

252271

α-Bromoisobutyryl bromide

Consecutive living polymerization from cationic to radical: a straightforward yet versatile methodology for the precision synthesis of ?cleavable? block copolymers with a hemiacetal ester junction.
Ouchi M, et al. et al.
Polym. Chem., 3, 2193-2199 (2012)
POLY (VINYLBENZYLPHOSPHONIC ACID)-BASED PROTON CONDUCTORS AS POLYMER ELECTROLYTE MEMBRANES FOR FUEL CELLS APPLICATIONS.
Polymer Preprints (American Chemical Society, Division of Polymer Chemistry), 49(1), 556-556 (2008)

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