物质信息

ID:717695

2-氯乙烷磺酰氯

名称和标识
IUPAC传统名
2-chloroethanesulfonyl chloride
IUPAC标准名
2-chloroethane-1-sulfonyl chloride
别名
2-Chloroethanesulfonyl chloride2-氯乙烷磺酰氯2-Chloroethylsulfonyl chloride
数据登录号
Beilstein号
CAS号
化合物性质
理化性质
密度
1.560
折射率
1.4915
闪点
>110°C(230°F)
沸点
203°C
安全信息
安全公开号
9-23-26-28-36/37/39-45
保存注意事项
Moisture Sensitive
GHS危险品标识
GHS05
腐蚀金属,类别1
腐蚀皮肤,类别1A,1B,1C
严重眼损伤,类别1
GHS06
急性毒性(口服,皮肤接触,吸入),类别1,2,3
危险公开号
22-26-34
GHS危险声明
H301-H330-H314-H318
欧盟危险性物质标志
剧毒 剧毒 (T+)
RTECS编号
KI8060000
GHS警示性声明
P260-P301+P310-P303+P361+P353-P304+P340-P305+P351+P338-P320-P330-P405-P501A
联合国危险货物等级
6.1
联合国危险货物包装类别(PG)
I
TSCA收录
联合国危险货物编号
UN3390
产品相关信息
纯度
98%
描述信息
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分子图谱
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参考文献
• In the presence of a base, converts alcohols to vinyl sulfonates: J. Am. Chem. Soc., 68, 1797 (1946); Angew. Chem. Int. Ed., 4, 300 (1965). These electrophilic alkenes readily undergo conjugate addition reactions with various nucleophiles:
• Reaction with pentafluorophenol, in the presence of Et3N, gives PFP vinylsulfonate, which can be converted to a sulfonamide via tin-mediated radical addition of alkyl halides to the olefinic bond, followed by displacement of the PFP group with an amine: Org. Lett., 42549 (2002).