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C69802

2-Chloropyridine

99%

Synonym(s):

α-Chloropyridine, o-Chloropyridine

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About This Item

Empirical Formula (Hill Notation):
C5H4ClN
CAS Number:
109-09-1
Molecular Weight:
113.54
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24892916
EC Number:
203-646-3
Beilstein/REAXYS Number:
105788
MDL number:
MFCD00006228
Assay:
99%
Form:
liquid
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vapor pressure

1.7 mmHg ( 20 °C)

Quality Level

100

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

wgk

WGK 3

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

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

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

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.

Poisonous substance

pdsc

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

fsl

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

C69802-VAR: + C69802-100G:4548173348797 + C69802-BULK: + C69802-RSAMPLE: + C69802-5G:4548173348810 + C69802-500G:4548173348803

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Certificates of Analysis (COA)

Lot/Batch Number
07114BJ
08017MH
05319JE
02030LP
07704ED

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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
David R Stapleton et al.
Journal of hazardous materials, 146(3), 640-645 (2007-06-05)
The degradation of 2-chloropyridine (2-CPY) and its degradation primary product 2-hydroxypyridine (2-HPY) was studied by means of ultraviolet (UV) irradiation at 254nm. Photolytic and photocatalytic experiments were conducted on 2-CPY and 2-HPY aqueous solutions in a batch reactor with internal
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
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