150514-48-0

Basic information

• Product Name: 4-(broMoMethyl)-N,N-diethylbenzaMide
• Synonyms: 4-(broMoMethyl)-N,N-diethylbenzaMide
• CAS NO: 150514-48-0
• Molecular Formula: C₁₂H₁₆BrNO
• Molecular Weight: 270.16554
• Mol File: 150514-48-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(broMoMethyl)-N,N-diethylbenzaMide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(broMoMethyl)-N,N-diethylbenzaMide(150514-48-0)
• EPA Substance Registry System: 4-(broMoMethyl)-N,N-diethylbenzaMide(150514-48-0)

Safety Data

• Hazardous Substances Data: 150514-48-0(Hazardous Substances Data)

Upstream product

• 79-37-8 oxalyl dichloride 
• 6232-88-8 4-bromomethylbenzoic Acid 
• 109-89-7 diethylamine 
• 52780-16-2 4-bromomethylbenzoyl chloride 

Downstream Products

• 150514-49-1 4-(1,4-Dioxa-8-azaspiro[4.5]dec-8-ylmethyl)-N,N-diethylbenzamide 
• 1189582-21-5 tert-Butyl 1-[4-(diethylcarbamoyl)benzyl]-3-(trifluoromethyl)-1,4,6,7-tetrahydro-5H-pyrazolo[4,3-c]pyridine-5-carboxylate 
• 1189582-15-7 tert-butyl 1-[4-(diethylcarbamoyl)benzyl]-3-(trifluoromethyl)-1,4,5,7-tetrahydro-6H-pyrazolo[3,4-c]pyridine-6-carboxylate 
• 1392825-44-3 N,N-diethyl-4-(4-iodo-3,3-dimethylbutyl)benzamide 

Relevant articles and documents

Nickel(0)/NaHMDS adduct-mediated intramolecular alkylation of unactivated arenes via a homolytic aromatic substitution mechanism

A variety of polycycles can be synthesized via an intramolecular alkylation cyclization promoted by Ni(PPh3)4 and NaHMDS. Mechanistic investigations support the catalytic nature of Ni0 in the course of TEMPO scavenging experiments and its association with the substrate and NaHMDS to form an adduct by DOSY NMR.