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132489

Sigma-Aldrich

2-Chloropyrazine

97%

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About This Item

Empirical Formula (Hill Notation):
C4H3ClN2
CAS Number:
14508-49-7
Molecular Weight:
114.53
Beilstein:
107019
EC Number:
238-517-0
MDL number:
MFCD00006124
UNSPSC Code:
12352100
eCl@ss:
39162102
PubChem Substance ID:
24848054
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.539 (lit.)

bp

153-154 °C (lit.)

density

1.283 g/mL at 25 °C (lit.)

functional group

chloro

SMILES string

Clc1cnccn1

InChI

1S/C4H3ClN2/c5-4-3-6-1-2-7-4/h1-3H

InChI key

GELVZYOEQVJIRR-UHFFFAOYSA-N

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Other Notes

remainder water

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Precautionary Statements

P210 - P370 + P378

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

134.6 °F - closed cup

Flash Point(C)

57 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

132489-BULK:
132489-VAR:
132489-25G:
132489-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP1246
MKCG3506
MKBW1028V
MKBV5000V
MKBQ7666V

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T J Wilke et al.
Journal of chromatography, 383(1), 77-83 (1986-11-28)
Diazohydroxide is a new antitumor agent being considered for clinical trial. A sensitive and specific assay for diazohydroxide in physiological media, plasma and blood has been developed based on conversion of diazohydroxide to 2-chloropyrazine in the presence of strong hydrochloric
Jeanne-Marie Bégouin et al.
The Journal of organic chemistry, 74(8), 3221-3224 (2009-03-25)
A cobalt-catalyzed cross-coupling of aryl halides with 2-chloropyrimidines or 2-chloropyrazines is reported in satisfactory to high yields. The key step of this procedure is the formation of aromatic organozinc reagents and their coupling with 2-chlorodiazines using the same cobalt halide

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