664774
4-Chlorobenzylsulfonyl chloride
97%
Synonym(s):
(4-Chlorophenyl)methanesulfonyl chloride, 4-Chlorobenzenemethanesulfonyl chloride, p-Chloro-α-toluenesulfonyl chloride
About This Item
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Assay
97%
form
solid
mp
93-97 °C
functional group
chloro
SMILES string
Clc1ccc(CS(Cl)(=O)=O)cc1
InChI
1S/C7H6Cl2O2S/c8-7-3-1-6(2-4-7)5-12(9,10)11/h1-4H,5H2
InChI key
DBJRPJSDYFDWPV-UHFFFAOYSA-N
Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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Articles
Sulfonyl chlorides are often chosen as building blocks in medicinal chemistry for their ability to easily react with heterocyclic amines to create complex sulfonamides.
Sulfonyl chlorides are often chosen as building blocks in medicinal chemistry for their ability to easily react with heterocyclic amines to create complex sulfonamides.
Sulfonyl chlorides are often chosen as building blocks in medicinal chemistry for their ability to easily react with heterocyclic amines to create complex sulfonamides.
Sulfonyl chlorides are often chosen as building blocks in medicinal chemistry for their ability to easily react with heterocyclic amines to create complex sulfonamides.
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