p-Toluenesulfinic acid

Details

Stereochemistry	ACHIRAL
Molecular Formula	C7H8O2S
Molecular Weight	156.202
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

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

InChI

InChIKey=FXJVNINSOKCNJP-UHFFFAOYSA-N

InChI=1S/C7H8O2S/c1-6-2-4-7(5-3-6)10(8)9/h2-5H,1H3,(H,8,9)

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
Base-induced photocyclization of 1,2-diaryl-1-tosylethenes. A mechanistically novel approach to phenanthrenes and phenanthrenoids.	2003 Dec 25	14682734
Highly selective palladium catalyzed kinetic resolution and enantioselective substitution of racemic allylic carbonates with sulfur nucleophiles: asymmetric synthesis of allylic sulfides, allylic sulfones, and allylic alcohols.	2003 Sep 5	12953206
Unsymmetrical diaryl sulfones and aryl vinyl sulfones through palladium-catalyzed coupling of aryl and vinyl halides or triflates with sulfinic acid salts.	2004 Aug 20	15307729
Analysis of eicosapentaenoic and docosahexaenoic acid geometrical isomers formed during fish oil deodorization.	2006 Sep 29	16893549
A highly stereoselective synthesis of (-)-(ent)-julifloridine from the cyclization of an alanine-derived chloroamine with an acetylenic sulfone.	2007 May 11	17439181

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Patents

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Name

Type

Language

BENZENESULFINIC ACID, 4-METHYL-

Preferred Name

English

p-Toluenesulfinic acid

Common Name

English

4-TOLUENESULFINIC ACID

Systematic Name

English

TOLUENE-4-SULPHINIC ACID

Systematic Name

English

4-METHYLBENZENESULFINIC ACID

Systematic Name

English

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Code System

Code

Type

Description

CAS

536-57-2

PRIMARY

MERCK INDEX

m10961

PRIMARY

Merck Index

EPA CompTox

DTXSID90862432

PRIMARY

PUBCHEM

10818

PRIMARY

MESH

C065428

PRIMARY

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SALT/SOLVATE (PARENT)


					7CKU5W4TRM

Sodium p-toluenesulfinic acid

SUBSTANCE RECORD


					H3F863QFL6

p-Toluenesulfinic acid