39066-09-6

Basic information

• Product Name: 2-(4-methoxy)-phenyl-butyronitrile
• Synonyms: 2-(4-methoxy)-phenyl-butyronitrile
• CAS NO: 39066-09-6
• Molecular Weight: 175.23
• Mol File: 39066-09-6.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-(4-methoxy)-phenyl-butyronitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxy)-phenyl-butyronitrile(39066-09-6)
• EPA Substance Registry System: 2-(4-methoxy)-phenyl-butyronitrile(39066-09-6)

Safety Data

• Hazardous Substances Data: 39066-09-6(Hazardous Substances Data)

Upstream product

• 1052267-76-1 2-(4-methoxy)-phenyl-but-2-enenitrile 
• 104-47-2 p-methoxybenzylnitrile 
• 64-17-5 ethanol 
• 75-03-6 ethyl iodide 
• 7677-24-9 trimethylsilyl cyanide 
• 5349-60-0 1-(4-methoxyphenyl)-1-propanol 
• 88932-42-7 4-methoxy-α-ethylbenzyl methyl ether 
• 123-11-5 4-methoxy-benzaldehyde 
• 140-67-0 Estragole 
• 77287-34-4 formamide 
• 104-46-1 anethole 

Downstream Products

• 51558-15-7 2-(4-methoxyphenyl)butan-1-amine 
• 205240-95-5 (S)-2-(4-Methoxy-phenyl)-butyric acid methyl ester 
• 131343-07-2 methyl 2-allyl-2-(p-methoxy)phenylacetate 
• 205241-11-8 (R)-2-(4-Methoxy-phenyl)-butyryl chloride 
• 205241-12-9 (S)-2-(4-Methoxy-phenyl)-butyryl chloride 
• 4646-94-0 (R)-2-(4-methoxyphenyl)butanoic acid 
• 13491-20-8 (S)-2-(4-methoxyphenyl)-butanoic acid 
• 4646-94-0 2-(4-methoxyphenyl)-n-butanoic acid 

Relevant articles and documents

α-Alkylation of Nitriles with Primary Alcohols by a Well-Defined Molecular Cobalt Catalyst

The α-alkylation of nitriles with primary alcohols to selectively synthesize nitriles by a well-defined molecular homogeneous cobalt catalyst is presented. Thirty-two examples with up to 95% yield are reported. Remarkably, this transformation is environmentally friendly and atom economical with water as the only byproduct.

DIHYDROISOQUINOLINE-2(1H)-CARBOXAMIDE AND RELATED COMPOUNDS AND THEIR USE IN TREATING MEDICAL CONDITIONS

The invention provides dihydroisoquinoline-2(1H)-carboxamide and related compounds, pharmaceutical compositions, and their use in the treatment of medical conditions, such as cancer, and in inhibiting HPK1 activity.

Efficient assembly of α-aryl and α-vinyl nitriles via iron-catalyzed ether bond activation

A novel and practical method for the synthesis of diverse α-aryl and α-vinyl nitriles was developed via an iron-catalyzed sp3 C-O ether bond cleavage with C-C bond formation in the reaction of π-activated ethers with TMSCN.