71681-37-3

Basic information

• Product Name: 3,4,5-trimethylbenzonitrile
• Synonyms: 3,4,5-trimethylbenzonitrile
• CAS NO: 71681-37-3
• Molecular Weight: 145.204
• Mol File: 71681-37-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3,4,5-trimethylbenzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5-trimethylbenzonitrile(71681-37-3)
• EPA Substance Registry System: 3,4,5-trimethylbenzonitrile(71681-37-3)

Safety Data

• Hazardous Substances Data: 71681-37-3(Hazardous Substances Data)

Upstream product

• 1660150-06-0 C₁₁H₁₂N₂O 
• 1639-31-2 3,4,5-trimethylaniline 
• 544-92-3 copper(I) cyanide 
• 1467-34-1 3',4',5'-trimethylacetanilide 

Downstream Products

• 13544-66-6 5-carbomethoxy-1,2,3-trimethylbenzene 
• 120743-87-5 3,5-dimethyl-4-<(trimethylsilyl)methyl>benzoic acid 
• 877774-32-8 [3,5-dimethyl-4-((trimethylsilyl)methyl)phenyl]methyl acetate 
• 877774-31-7 3,5-dimethyl-4-[(trimethylsilyl)methyl]benzyl alcohol 
• 877774-21-5 2,5-dimethyl-p-xylylene 
• 1076-88-6 3,4,5-trimethylbenzoic acid 

Relevant articles and documents

A base-induced ring-opening process of 2-substituted-1,3,4-oxadiazoles for the generation of nitriles at room temperature

A novel base-catalysed 1,3,4-oxadiazole fragmentation for the synthesis of nitriles at room temperature has been developed. This reaction is performed under transition-metal-free conditions, and provides a new ring cleavage reaction of 1,3,4-oxadiazoles in organic synthesis.