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2-氯苯磺酰胺

规格或纯度: ≥98.0%(GC)
有货

库存信息

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库存信息

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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
C137002-5g
5g 现货 Stock Image
C137002-25g
25g 现货 Stock Image
C137002-100g
100g 现货 Stock Image
C137002-500g
500g 现货 Stock Image
C137002-2.5kg
2.5kg 现货 Stock Image

基本描述

别名 邻氯苯磺酰胺
英文别名 2-Chlorobenzenesulfonamide|6961-82-6|o-Chlorobenzenesulfonamide|Benzenesulfonamide, 2-chloro-|2-chlorobenzene-1-sulfonamide|Benzenesulfonamide, o-chloro-|2-CHLOROBENZENESULPHONAMIDE|2-chlorophenylsulfonamide|2-Chloro-benzenesulfonamide|4BT2I28A0C|DTXSID20
规格或纯度 ≥98.0%(GC)
英文名称 2-Chlorobenzenesulfonamide
应用 2-Chlorobenzenesulfonamide may be used in the synthesis of 2-chloro-N-(4-methoxybenzoyl)benzenesulfonamide and 1,2,4-thiadiazine [1],1-dioxides.
运输条件 常规运输
备注 500g卖完停产,不再备货
产品介绍

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. 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.

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.

名称和标识符

PubChem SID 488185961
PubChem SID url https://pubchem.ncbi.nlm.nih.gov/substance/488185961
IUPAC Name 2-chlorobenzenesulfonamide
INCHI 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
Canonical SMILES C1=CC=C(C(=C1)S(=O)(=O)N)Cl
Isomeric SMILES C1=CC=C(C(=C1)S(=O)(=O)N)Cl
WGK Germany 3
PubChem CID 81410
分子量 191.63
Beilstein号 11(3)88
Reaxy-Rn 2937540

化学和物理性质

溶解性 不溶于水
熔点 187-192°C

安全和危险性(GHS)

象形图
ghs07

Harmful

信号词 Warning
危险声明 H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
预防措施声明 P261,P305+P351+P338,P280,P302+P352,P321,P405,P501,P264,P271,P304+P340,P403+P233,P362+P364,P264+P265,P337+P317,P332+P317,P319
WGK Germany 3
Reaxy-Rn 2937540
个人防护装备 dust mask type N95 (US), Eyeshields, Gloves

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参考文献

1. E R Ventre.  (1985-09-27)  Determination of the content of 2-chlorobenzenesulphonamide and bis(p-chlorophenyl) sulphone in 4-chlorobenzenesulphonamide..  Journal of chromatography,  333  ((1)):  (253-255).  [PMID:4066841]
2. H P Hershey,T D Stoner.  (1991-10-01)  Isolation and characterization of cDNA clones for RNA species induced by substituted benzenesulfonamides in corn..  Plant molecular biology,  17  ((4)):  (679-690).  [PMID:1912492]
3. Aldo Pagano,Manuele Castelnuovo,Federico Tortelli,Roberto Ferrari,Giorgio Dieci,Ranieri Cancedda.  (2007-02-06)  New small nuclear RNA gene-like transcriptional units as sources of regulatory transcripts..  PLoS genetics,  ((2)):  (e1-e1).  [PMID:17274687]