METHANESULFONYL CHLORIDE

Details

Stereochemistry	ACHIRAL
Molecular Formula	CH3ClO2S
Molecular Weight	114.551
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

CS(Cl)(=O)=O

InChI

InChIKey=QARBMVPHQWIHKH-UHFFFAOYSA-N

InChI=1S/CH3ClO2S/c1-5(2,3)4/h1H3

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Approval Year

PubMed

Show entries

Title	Date	PubMed
Novel azido fatty acid ester derivatives from conjugated C(18) enynoate.	2001 May	11438282
A new type of mixed anhydride and its applications to the synthesis of 7-substituted 8-chloro-5,5-dioxoimidazo[1,2-b][1,4,2]benzodithiazines with in vitro antitumor activity.	2002 Jan 17	11784147
A convenient method for the conversion of hindered carboxylic acids to N-methoxy-N-methyl (Weinreb) amides.	2004 Dec 10	15575791
Synthesis, molecular structure and reactivity of 5-methylidene-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolines.	2004 Feb 28	18007413
Conjugation of amino-containing drugs to polysaccharides by tosylation: amphotericin B-arabinogalactan conjugates.	2004 Jul	14967538

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Name

Type

Language

METHANESULFONYL CHLORIDE

Systematic Name

English

METHANESULFONYL CHLORIDE [HSDB]

Common Name

English

METHANESULFONYL CHLORIDE [MI]

Common Name

English

MESYL CHLORIDE

Systematic Name

English

NSC-15039

Code

English

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Code System

Code

Type

Description

MESH

C030209

PRIMARY

NSC

15039

PRIMARY

WIKIPEDIA

METHANESULFONYL CHLORIDE

PRIMARY

PUBCHEM

31297

PRIMARY

EPA CompTox

DTXSID1021615

PRIMARY

Showing 1 to 5 of 10 entries

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SUBSTANCE RECORD


					B17EWY1R7Q

METHANESULFONYL CHLORIDE

SMILES

InChI

Approval Year

PubMed

Patents