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Merck

C69802

2-Chloropyridine

99%

동의어(들):

α-Chloropyridine, o-Chloropyridine

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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C5H4ClN
CAS 번호:
Molecular Weight:
113.54
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-646-3
Beilstein/REAXYS Number:
105788
MDL number:
Assay:
99%
Form:
liquid
기술 서비스
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도움 문의

InChI key

OKDGRDCXVWSXDC-UHFFFAOYSA-N

InChI

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

SMILES string

Clc1ccccn1

vapor pressure

1.7 mmHg ( 20 °C)

assay

99%

form

liquid

Quality Level

refractive index

n20/D 1.532 (lit.)

bp

166 °C/714 mmHg (lit.)

density

1.2 g/mL at 25 °C (lit.)

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

저장 등급

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

wgk

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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시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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
Mattia Moiola et al.
ChemistryOpen, 9(2), 195-199 (2020-02-07)
1,2,4-Oxadiazole[4,5-a]piridinium salts add alcohols and alkoxides to undergo electrocyclic ring opening affording alkoxybutadienyl 1,2,4-oxadiazole derivatives. The pyridinium salts represent a special class of Zincke salts that are prone to rearrange to give alkoxybutadienyl 1,2,4-oxadiazoles when treated with suitable nucleophiles or
Dimitris Vlastos et al.
Journal of hazardous materials, 177(1-3), 892-898 (2010-01-20)
2-Chloropyridine (2-CPY) has been identified as a trace organic chemical in process streams, wastewater and even drinking water. Furthermore, it appears to be formed as a secondary pollutant during the decomposition of specific insecticides. As reported in our previous work
Trevor J Dines et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(13), 3205-3217 (2003-10-30)
The adsorption of 2-chloropyridine on SiO(2), TiO(2), ZrO(2), SiO(2)-Al(2)O(3) and H-mordenite has been studied by IR spectroscopy. The different modes of interaction with oxide surfaces, i.e. hydrogen-bonding and adsorption at Brønsted or Lewis acid sites, was modelled by ab initio

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