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C69802

Sigma-Aldrich

2-Chloropyridine

99%

Sinónimos:

α-Chloropyridine, o-Chloropyridine

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About This Item

Fórmula empírica (notación de Hill):
C5H4ClN
Número de CAS:
109-09-1
Peso molecular:
113.54
Beilstein/REAXYS Number:
105788
EC Number:
203-646-3
MDL number:
MFCD00006228
UNSPSC Code:
12352100
PubChem Substance ID:
24892916
NACRES:
NA.22

vapor pressure

1.7 mmHg ( 20 °C)

assay

99%

form

liquid

refractive index

n20/D 1.532 (lit.)

bp

166 °C/714 mmHg (lit.)

density

1.2 g/mL at 25 °C (lit.)

SMILES string

Clc1ccccn1

InChI

1S/C5H4ClN/c6-5-3-1-2-4-7-5/h1-4H

InChI key

OKDGRDCXVWSXDC-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

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

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Andreas Reichelt et al.
Organic letters, 12(4), 792-795 (2010-01-27)
An efficient and convenient method for the synthesis of [1,2,4]triazolo[4,3-a]pyridines was exemplified by the synthesis of 20 analogues bearing a variety of substituents at the 3-position. The methodology involves a palladium-catalyzed addition of hydrazides to 2-chloropyridine, which occurs chemoselectively at
Contribution of N-oxidation and .OH radicals to mutagenesis of 2-chloropyridine in Salmonella typhimurium.
B Chłopkiewicz et al.
Acta biochimica Polonica, 40(1), 57-59 (1993-01-01)
Fereshteh Mehri et al.
Iranian journal of pharmaceutical research : IJPR, 19(4), 143-150 (2021-04-13)
A sensitive method using ion-pair extraction was developed by liquid chromatography tandem mass spectrometry (LC-MS/MS) for measurement of 4-methylimidazole (4-MI) in NMRI mice plasma and cerebrospinal fluid (CSF). Detection was done by electrospray positive ionization mass spectrometry in the multiple-reaction
David R Stapleton et al.
Water research, 43(16), 3964-3973 (2009-07-14)
The photolytic destruction and mineralisation of 2-halogenated pyridines (2-HalPYs) was studied in a range of conditions by means of ultraviolet irradiation at 254 nm. In all cases pseudo-first order kinetics satisfactorily describe the degradation process. Key decomposition products were identified
Kazuko Inoue et al.
Drug metabolism and disposition: the biological fate of chemicals, 37(9), 1797-1800 (2009-06-23)
We investigated the substitution reaction of a series of 2-chloropyridine derivatives catalyzed by rat liver microsomal glutathione S-transferase 1. Various 2-chloropyridine derivatives were metabolized to the corresponding substituted glutathione conjugates via displacement of chlorine atom with glutathione. The reaction was
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