70916-14-2

Basic information

• Product Name: triethyl-(2-oxo-2-phenylethyl)ammonium bromide
• Synonyms: triethyl-(2-oxo-2-phenylethyl)ammonium bromide
• CAS NO: 70916-14-2
• Molecular Weight: 300.239
• Mol File: 70916-14-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: triethyl-(2-oxo-2-phenylethyl)ammonium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: triethyl-(2-oxo-2-phenylethyl)ammonium bromide(70916-14-2)
• EPA Substance Registry System: triethyl-(2-oxo-2-phenylethyl)ammonium bromide(70916-14-2)

Safety Data

• Hazardous Substances Data: 70916-14-2(Hazardous Substances Data)

Upstream product

• 121-44-8 triethylamine 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 1074-12-0 phenylglyoxal hydrate 
• 121-44-8 triethylamine 

Relevant articles and documents

Rhodium-catalyzed C-H activation of phenacyl ammonium salts assisted by an oxidizing C-N bond: A combination of experimental and theoretical studies

Rh(III)-catalyzed C-H activation assisted by an oxidizing directing group has evolved to a mild and redox-economic strategy for the construction of heterocycles. Despite the success, these coupling systems are currently limited to cleavage of an oxidizing

NOVEL FLUORINATED ALKYLFLUOROPHOSPHORIC ACID SALT OF ONIUM AND TRANSITION METAL COMPLEX

[Problems] To obtain a polymerization initiator (acid generating agent) having excellent power for initiation of cationic polymerization without containing arsenic or antimony. [Means for solution] Provided is a specific onium salt or transition metal complex salt of a fluorinated alkyl fluorophosphoric acid.

Effect of addition of phenols on the rate of Menschutkin reaction-Reaction between phenacyl bromide and triethylamine

Second order rate constants for the reaction between phenacyl bromide and triethylamine with and without phenols have been determined in aprotic solvents at 25 deg, 30 deg and 35 deg C.The addition of X-C6H4-OH (X=H, p-OCH3, p-CH3, p-Cl, p-Br and p-NO2) w