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方案
98%
mp
189-193 °C (lit.)
SMILES字符串
NS(=O)(=O)c1ccccc1Cl
InChI
1S/C6H6ClNO2S/c7-5-3-1-2-4-6(5)11(8,9)10/h1-4H,(H2,8,9,10)
InChI key
JCCBZCMSYUSCFM-UHFFFAOYSA-N
一般描述
2-Chlorobenzenesulfonamide is a halogenated sulfonamide derivative. It is formed as one of the major degradation product of chlorosulfuron. Crystals of 2-chlorobenzenesulfonamide exhibit monoclinic space group Cc. Its molecules are linked by N1—H11···O1 and N1—H12···O2 hydrogen bonding to form an infinite 3-D molecular network.
应用
2-Chlorobenzenesulfonamide may be used in the synthesis of 2-chloro-N-(4-methoxybenzoyl)benzenesulfonamide and 1,2,4-thiadiazine ,1-dioxides.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Synthesis and biological activity of novel 3-heteroaryl-2H-pyrido [4, 3-e][1, 2, 4] thiadiazine and 3-heteroaryl-2H-benzo [e][1, 2, 4] thiadiazine 1, 1-dioxides.
Gobis, Katarzyna, et al.
Monatshefte fur Chemie / Chemical Monthly, 144(8), 1197-1203 (2013)
2-Chlorobenzenesulfonamide.
Gowda BT, et al.
Acta Crystallographica Section E, Structure Reports Online, 65(9), o2144-o2144 (2009)
Aldo Pagano et al.
PLoS genetics, 3(2), e1-e1 (2007-02-06)
By means of a computer search for upstream promoter elements (distal sequence element and proximal sequence element) typical of small nuclear RNA genes, we have identified in the human genome a number of previously unrecognized, putative transcription units whose predicted
2-Chloro-N-(4-methoxybenzoyl) benzenesulfonamide.
Sreenivasa S, et al.
Acta Crystallographica Section E, Structure Reports Online, 70(2), o199-o199 (2014)
Fate of chlorsulfuron in the environment. 2. Field evaluations.
Strek HJ.
Pestic. Sci., 53(1), 52-70 (1998)
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