产品名称
2-氯苯磺酰胺, 98%
InChI key
JCCBZCMSYUSCFM-UHFFFAOYSA-N
InChI
1S/C6H6ClNO2S/c7-5-3-1-2-4-6(5)11(8,9)10/h1-4H,(H2,8,9,10)
SMILES string
NS(=O)(=O)c1ccccc1Cl
assay
98%
mp
189-193 °C (lit.)
Application
2-Chlorobenzenesulfonamide may be used in the synthesis of 2-chloro-N-(4-methoxybenzoyl)benzenesulfonamide and 1,2,4-thiadiazine ,1-dioxides.
General description
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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-Chlorobenzenesulfonamide.
Gowda BT, et al.
Acta Crystallographica Section E, Structure Reports Online, 65(9), o2144-o2144 (2009)
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)
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
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