119306-02-4

Basic information

• Product Name: geranyl p-toluenesulfinate
• Synonyms: geranyl p-toluenesulfinate
• CAS NO: 119306-02-4
• Molecular Weight: 292.442
• Mol File: 119306-02-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: geranyl p-toluenesulfinate(CAS DataBase Reference)
• NIST Chemistry Reference: geranyl p-toluenesulfinate(119306-02-4)
• EPA Substance Registry System: geranyl p-toluenesulfinate(119306-02-4)

Safety Data

• Hazardous Substances Data: 119306-02-4(Hazardous Substances Data)

Upstream product

• 10439-23-3 4-methylbenzenesulfinyl chloride 
• 106-24-1 Geraniol 
• 536-57-2 p-toluene sulfinic acid 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 5389-87-7 1-chloro-3,7-dimethylocta-2,6-diene 
• 21179-27-1 (S)-(+)-N,N,4-trimethylbenzenesulfinamide 
• 106-25-2 Nerol 

Downstream Products

• 72863-23-1 3,7-dimethyl-3-(p-tolylsulfonyl)-1,6-octadiene 
• 53254-60-7 3,7-dimethyl-1-(p-toluenesulfonyl)-2(E),6-octadiene 
• 130265-09-7 1-((S)-3,7-Dimethyl-octa-1,6-diene-3-sulfonyl)-4-methyl-benzene 
• 130265-15-5 1-((R)-3,7-Dimethyl-octa-1,6-diene-3-sulfonyl)-4-methyl-benzene 

Relevant articles and documents

Isocyanide-Induced Esterification of Sulfinic Acids to Access Sulfinates

The isocyanide-induced esterification of sulfinic acids with alcohols or thiophenols access to sulfinates has been developed. Various primary, secondary, and tertiary alcohols could be compatible with the established protocols. Notably, such an isocyanide-induced synthetic strategy presented the advantages of simple operation, good functional group tolerance, and more than 40 examples up to 99% yields. (Figure presented.).

Synthesis of three acyclic all-trans-tetraterpene diols, putative precursors of bacterial lipids

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