Weight | 114.553 g/mol |
---|---|
Formula | CH3ClO2S |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Methanesulfonyl chloride (124-63-0)
methanesulfonyl chloride, 37Cl-labeled · methanesulfonyl chloride, 35S-labeled · methanesulfonyl chloride, 35Cl-labeled
Score:
#775 in Physics
,
#2241 in Chemistry
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- Preparation of methanesulfonyl chloride. (Journal of the American Chemical Society, 1948)
- FriedelCrafts Reactions of Methanesulfonyl Chloride with Benzene and Certain Substituted Benzenes1 (Journal of the American Chemical Society, 1953)
- Sulfene, an Intermediate in the Alcoholysis of Methanesulfonyl Chloride (Journal of the American Chemical Society, 1964)
- Rate and product studies in the solvolyses of methanesulfonic anhydride and a comparison with methanesulfonyl chloride solvolyses (Journal of Physical Organic Chemistry, 2007)
- On the Methylation of Carboxyl Groups with Methanesulfonyl Chloride in Pyridine. (Synthetic Communications, 2003)
- An efficient -amino acid cyclodehydration using methanesulfonyl chloride to thienamycin intermediate 3-[1-hydroxyethyl]-4-[methoxy carbonylmethyl]-azetidin-2-one (Tetrahedron Letters, 1991)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H402: Harmful to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 3 - methanesulfonyl chloride, 37Cl-labeled
- methanesulfonyl chloride, 35S-labeled
- methanesulfonyl chloride, 35Cl-labeled
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SMILESCS(=O)(=O)Cl
-
InChIKeyQARBMVPHQWIHKH-UHFFFAOYSA-N
- Pubchem - Methanesulfonyl chloride
- Wikipedia - methanesulfonyl chloride
Methanesulfonyl chloride (mesyl chloride) is an organosulfur compound with the formula CH3SO2Cl. It is a colourless liquid that dissolves in polar organic solvents but is reactive toward water, alcohols, and many amines. The simplest organic sulfonyl chloride, it is used to make methanesulfonates and to generate the elusive molecule sulfene.
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Ethanesulfonamide
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methanesulfonohydrazide
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Methanesulfonic anhydride
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Propyl sulfone
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Isopropylsulfamoyl chloride
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2-(4-METHYLPHENOXY)ETHANESULFONYL CHLORIDE
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butane-1-sulfonamide
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butane-1,4-disulfonic acid
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