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About This Item
线性分子式:
F2C6H3SO2Cl
CAS号:
分子量:
212.60
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
97%
折射率
n20/D 1.526 (lit.)
沸点
210 °C (lit.)
密度
1.568 g/mL at 25 °C (lit.)
SMILES字符串
Fc1cccc(F)c1S(Cl)(=O)=O
InChI
1S/C6H3ClF2O2S/c7-12(10,11)6-4(8)2-1-3-5(6)9/h1-3H
InChI key
QXWAUQMMMIMLTO-UHFFFAOYSA-N
一般描述
2,6-Difluorobenzenesulfonyl chloride can be prepared by reacting difluorophenyllithium with sulfuryl chloride.
应用
2,6-Difluorobenzenesulfonyl chloride may be used in the synthesis of 2,6-difluorobenzenesulfonamide and benzoxathiazocine 1,1-dioxides core scaffolds.
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Insect growth regulators. Analogues of TH-6038 and TH-6040.
J E Oliver et al.
Journal of agricultural and food chemistry, 24(5), 1065-1068 (1976-09-01)
Joanna K Loh et al.
Beilstein journal of organic chemistry, 8, 1293-1302 (2012-09-29)
The efficient synthesis of an 80-member library of unique benzoxathiazocine 1,1-dioxides by a microwave-assisted, intermolecular nucleophilic aromatic substitution (S(N)Ar) diversification pathway is reported. Eight benzofused sultam cores were generated by means of a sulfonylation/S(N)Ar/Mitsunobu reaction pairing protocol, and subsequently diversified
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