化驗
90%
雜質
10% 2-chlorobenzenesulfonyl chloride
折射率
n20/D 1.559 (lit.)
bp
285 °C (lit.)
密度
1.484 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
Clc1ccccc1S(=O)(=O)N=C=O
InChI
1S/C7H4ClNO3S/c8-6-3-1-2-4-7(6)13(11,12)9-5-10/h1-4H
InChI 密鑰
LALCDSDHLXWTTL-UHFFFAOYSA-N
一般說明
2-Chlorobenzenesulfonyl isocyanate is an aryl isocyanate that can be synthesized by the catalytic carbonylation of potassium N,2- dichlorobenzenesulfonamidate in acetonitrile. The C-acylation of nitrogen bearing heterocycles using 2-chlorobenzenesulfonyl isocyanate has been reported.
應用
2-Chlorobenzenesulfonyl isocyanate may be used in the synthesis of N-thiazolyl-N′-(2-chlorobenzenesulfonyl)urea derivatives and N-(2-chlorophenylsulfonyl)-N′-(4-methoxy-6-methyl-triazin-2-yl)urea.
訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
235.4 °F - closed cup
閃點(°C)
113 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Thiazolecarboxylic acid derivatives. 1. N-substituted 2-amino-4-methylthiazole-5-carboxylic acid derivatives.
Chemistry of Heterocyclic Compounds, 40(1), 84-89 (2004)
Catalytic carbonylation of potassium N,2-dichlorobenzenesulfonamidate to sulfonyl isocyanate.
Reaction Kinetics and Catalysis Letters, 62(2), 321-326 (1997)
C-Acylation of Electron-Rich Heterocycles by o-Chlorobenzenesulfonyl Isocyanate.
ChemInform, 27(35) (1996)
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