Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

C22369

Sigma-Aldrich

2-Chloroacrylonitrile

98%

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

About This Item

Linear Formula:
CH2=CClCN
CAS Number:
920-37-6
Molecular Weight:
87.51
Beilstein:
773744
MDL number:
MFCD00001858
UNSPSC Code:
12352100
PubChem Substance ID:
24892478
NACRES:
NA.22

Quality Level

200

Assay

98%

form

liquid

refractive index

n20/D 1.429 (lit.)

bp

88-89 °C (lit.)

mp

−65 °C (lit.)

density

1.096 g/mL at 25 °C (lit.)

SMILES string

ClC(=C)C#N

InChI

1S/C3H2ClN/c1-3(4)2-5/h1H2

InChI key

OYUNTGBISCIYPW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Common reagent in cycloaddition reactions.

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 3 - Carc. 1B - Eye Dam. 1 - Flam. Liq. 2 - Resp. Sens. 1 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

42.8 °F - closed cup

Flash Point(C)

6 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKBN6229V
BCBF8760V
MKBH5728
BCBF8760
STBC1511

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Journal of the Chemical Society. Chemical Communications, 814-814 (1993)
The Journal of Organic Chemistry, 58, 5200-5200 (1993)
A G Craan et al.
Toxicology, 56(1), 47-61 (1989-05-31)
The nephrotoxicity of glutathione (GSH) pathway metabolites derived from toluene (TOL), styrene (STYR), bromobenzene (BB), acrylonitrile (ACLN) and 2-chloroacrylonitrile (CACLN) were compared with that of dichlorovinylcysteine (DCVC), using renal brush border and basal-lateral uptake parameters as indices. Cysteine conjugates and
Yi Wang et al.
Journal of the American Chemical Society, 128(12), 3928-3930 (2006-03-23)
Catalytic tandem asymmetric reactions constitute a powerful strategy for the asymmetric construction of nonadjacent stereocenters in acyclic molecules directly from achiral precursors. In this Communication, we report a highly enantioselective and diastereoselective addition of trisubstituted carbon donors to 2-chloroacrylonitrile catalyzed
[Information from the Soviet Toxicology Center].
Gigiena truda i professional'nye zabolevaniia, (2)(2), 52-53 (1983-02-01)
View All Related Papers

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