C69802
2-クロロピリジン
99%
別名:
α-Chloropyridine, o-Chloropyridine
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この商品について
実験式（ヒル表記法）:
C5H4ClN
CAS番号:
分子量:
113.54
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-646-3
Beilstein/REAXYS Number:
105788
MDL number:
製品名
2-クロロピリジン, 99%
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
refractive index
n20/D 1.532 (lit.)
bp
166 °C/714 mmHg (lit.)
density
1.2 g/mL at 25 °C (lit.)
Quality Level
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関連するカテゴリー
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
保管分類
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
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
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
Michał Gągol et al.
Ultrasonics sonochemistry, 45, 257-266 (2018-05-01)
Cavitation has become on the most often applied methods in a number of industrial technologies. In the case of oxidation of organic pollutants occurring in the aqueous medium, cavitation forms the basis of numerous advanced oxidation processes (AOPs). This paper
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
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)
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