10531-13-2

Usage

Uses

Used in Chemical Synthesis:
Cyanomethyl benzenesulfonate is used as a cyanomethylating agent for the synthesis of nido-and closo-arsacarboranes. It plays a crucial role in the formation of these complex chemical structures, which have potential applications in various fields.
Used in Analytical Chemistry:
Cyanomethyl benzenesulfonate is used in the separation of aromatic hydrophobic sulfonates by micellar electrokinetic chromatography. This technique utilizes different buffer systems to effectively separate and analyze these compounds, which is essential for understanding their properties and potential applications.

InChI:InChI=1/C8H7NO3S/c9-6-7-12-13(10,11)8-4-2-1-3-5-8/h1-5H,7H2

Upstream product

• 107-16-4 glycolonitrile 
• 98-09-9 benzenesulfonyl chloride 
• 50-00-0 formaldehyd 
• 143-33-9 sodium cyanide 
• 151-50-8 potassium cyanide 

Downstream Products

• 34688-71-6 mesitylacetonitrile 
• 4408-60-0 2-mesitylacetic acid 
• 105556-78-3 Benzenesulfonate(1R,2S)-2-benzyloxymethyl-1-cyanomethyl-1-((E)-3-p-tolyl-but-2-enyl)-pyrrolidinium; 
• 623-49-4 ethyl cyanoformate 
• 63720-80-9 2-(N-Ethyl-2-chloranilino)acetonitril 
• 90909-44-7 benzenesulfonyloxy-acetic acid 
• 90909-43-6 benzenesulfonyloxy-acetic acid methyl ester 

Relevant academic research and scientific papers

Scavenger assisted combinatorial process for preparing libraries of tertiary amine compounds

This invention relates to a novel solution phase process for the preparation of tertiary amine combinatorial libraries. These libraries have utility for drug discovery and are used to form wellplate components of novel assay kits.

Process for the preparation of optionally-substituted 1,2,3,4-tetrahydro-9-cyanomethylcarbazol-1-ones

In a process for the preparation of optionally-substituted 1,2,3,4-tetrahydro-9-cyanomethylcarbazol-1-ones of the formula STR1 wherein R denotes hydrogen, halogen, alkyl or alkoxy, by cyano-methylating optionally substituted 1,2,3,4-tetrahydrocarbazol-1-ones of the formula STR2 wherein R has the meanings mentioned above, the starting material of formula II is reacted, in a two-phase system consisting of water and a water-immiscible organic solvent, in the presence of a strong base and a known phase transfer catalyst, with a cyanomethylating agent of the formula wherein R1 denotes halogen or a radical of the formula R2 --SO2 --O-- and R2 represents alkyl, phenyl or substituted phenyl.

Method of protecting plants from pathogens with cyanomethyl aryl sulfonates

Fungi or bacteria pathogenic to plants are inhibited by applying to the locus to be protected therefrom a biocidally effective amount of a cyanomethyl arylsulfonate represented by the formula RSO3 CH2 CN where R is STR1