M-TOLUENESULPHONAMIDE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C7H9NO2S
Molecular Weight	171.217
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of M-TOLUENESULPHONAMIDE

Structure Search

SMILES

CC1=CC=CC(=C1)S(N)(=O)=O

InChI

InChIKey=NVZINPVISUVPHW-UHFFFAOYSA-N

InChI=1S/C7H9NO2S/c1-6-3-2-4-7(5-6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

Title	Date	PubMed
Carbonic anhydrase inhibitors: anticonvulsant sulfonamides incorporating valproyl and other lipophilic moieties.	2002-01-17	11784136
(N-[2-(eta[5]cyclopentadienyl)ethyl]-4-toluenesulfonamido-N,O)(tetrahydrofuran-O)bis(trifluoromethanesulfonato-O)titanium(II).	2001-04	11313560

Patents

Patents

Name

Type

Language

3-METHYLBENZENESULFONAMIDE

Preferred Name

English

M-TOLUENESULPHONAMIDE

Systematic Name

English

3-TOLUENESULPHONAMIDE

Systematic Name

English

3-TOLUENESULFONAMIDE

Systematic Name

English

M-METHYLBENZENESULFONAMIDE

Systematic Name

English

BENZENESULFONAMIDE, 3-METHYL-

Systematic Name

English

M-TOLUENESULFONAMIDE

Systematic Name

English

Code System Code Type Description

CAS

1899-94-1

Created by admin on Mon Mar 31 22:38:32 GMT 2025 , Edited by admin on Mon Mar 31 22:38:32 GMT 2025

PRIMARY

EPA CompTox

DTXSID40172417

Created by admin on Mon Mar 31 22:38:32 GMT 2025 , Edited by admin on Mon Mar 31 22:38:32 GMT 2025

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PUBCHEM

74697

Created by admin on Mon Mar 31 22:38:32 GMT 2025 , Edited by admin on Mon Mar 31 22:38:32 GMT 2025

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FDA UNII

M2228F53M9

Created by admin on Mon Mar 31 22:38:32 GMT 2025 , Edited by admin on Mon Mar 31 22:38:32 GMT 2025

PRIMARY

ECHA (EC/EINECS)

217-596-5

Created by admin on Mon Mar 31 22:38:32 GMT 2025 , Edited by admin on Mon Mar 31 22:38:32 GMT 2025

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SUBSTANCE RECORD


					M2228F53M9

M-TOLUENESULPHONAMIDE