TOSYLMETHYL ISOCYANIDE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C9H9NO2S
Molecular Weight	195.238
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)C[N+]#[C-]

InChI

InChIKey=CFOAUYCPAUGDFF-UHFFFAOYSA-N

InChI=1S/C9H9NO2S/c1-8-3-5-9(6-4-8)13(11,12)7-10-2/h3-6H,7H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
Reaction of bromomethylazoles and tosylmethyl isocyanide. A novel heterocyclization method for the synthesis of the core of marine alkaloids variolins and related azolopyrimidines.	2004 Jul 23	15255724
Synthesis and biological activity of a new class of sulfone-linked pyrrolylpyrazoles and pyrrolylisoxazoles from methyl-3-aryl-2-(E-arylethenesulfonyl)acrylate.	2009 Nov	19881267
Condensation reactions to form oxazoline-substituted potassium organotrifluoroborates.	2009 Sep 3	19708697
4-Phenyl-sulfon-yl-2-(p-tolyl-sulfon-yl)-1H,8H-pyrrolo-[2,3-b]indole.	2010 Oct 9	21588961

Showing 1 to 4 of 4 entries

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Patents

Show entries

Name

Type

Language

TOSYLMETHYL ISOCYANIDE

Systematic Name

English

4-TOLUENESULFONYLMETHYL ISOCYANIDE

Systematic Name

English

TOSYLMETHYL ISOCYANIDE [MI]

Common Name

English

P-TOLUENESULFONYLMETHYL ISOCYANIDE

Common Name

English

TOSMIC

Common Name

English

Showing 1 to 5 of 13 entries

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Code System

Code

Type

Description

NSC

631633

PRIMARY

EPA CompTox

DTXSID90190101

PRIMARY

PUBCHEM

161915

PRIMARY

WIKIPEDIA

TOSMIC

PRIMARY

MERCK INDEX

m10985

PRIMARY

Merck Index

Showing 1 to 5 of 8 entries

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SUBSTANCE RECORD


					C35FD6OLH8

TOSYLMETHYL ISOCYANIDE