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
Fate of chlorsulfuron in the environment. 2. Field evaluations.
Strek HJ.
Pestic. Sci., 53(1), 52-70 (1998)
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)
H P Hershey et al.
Plant molecular biology, 17(4), 679-690 (1991-10-01)
A search of compounds capable of inducing specific gene expression in plants without affecting growth and development led to the examination of changes in the pattern of gene expression in corn after treatment with substituted benzenesulfonamide herbicide safeners. Following hydroponic
2-Chloro-N-(4-methoxybenzoyl) benzenesulfonamide.
Sreenivasa S, et al.
Acta Crystallographica Section E, Structure Reports Online, 70(2), o199-o199 (2014)
2-Chlorobenzenesulfonamide.
Gowda BT, et al.
Acta Crystallographica Section E, Structure Reports Online, 65(9), o2144-o2144 (2009)
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