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蒸汽压
1.7 mmHg ( 20 °C)
质量水平
检测方案
99%
形式
liquid
折射率
n20/D 1.532 (lit.)
bp
166 °C/714 mmHg (lit.)
密度
1.2 g/mL at 25 °C (lit.)
SMILES字符串
Clc1ccccn1
InChI
1S/C5H4ClN/c6-5-3-1-2-4-7-5/h1-4H
InChI key
OKDGRDCXVWSXDC-UHFFFAOYSA-N
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警示用语：
Danger
危险分类
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
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
154.4 °F
闪点(°C)
68 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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
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)
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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