260783-80-0

Basic information

• Product Name: N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate
• Synonyms: N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate
• CAS NO: 260783-80-0
• Molecular Weight: 299.314
• Mol File: 260783-80-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate(260783-80-0)
• EPA Substance Registry System: N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate(260783-80-0)

Safety Data

• Hazardous Substances Data: 260783-80-0(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 50-00-0 formaldehyd 
• 100-46-9 benzylamine 
• 333-27-7 methyl trifluoromethanesulfonate 
• 124-40-3 dimethyl amine 
• 103-83-3 N,N'-dimethylbenzylamine 
• 191666-77-0 [Cp(*)Ir(η(3)-CHPhCHCH2)(NCMe)](OTf) 
• 100-44-7 benzyl chloride 
• 75-50-3 trimethylamine 

Downstream Products

• 620-83-7 1-methyl-4-(phenylmethyl)benzene 
• 101-81-5 Diphenylmethane 
• 834-14-0 p-benzylanizole 
• 587-79-1 4-fluorodiphenylmethane 
• 23450-30-8 methyl 4-benzylbenzoate 
• 1416981-80-0 4-benzyl-N-cyclopentylbenzamide 
• 34239-04-8 1-benzyl-4-(trifluoromethyl)benzene 
• 883-90-9 o-benzyl anisole 
• 28994-41-4 o-Benzylphenol 
• 3794-15-8 1-benzyl-2-fluorobenzene 
• 1496-00-0 1-benzyl-3-fluorobenzene 
• 23450-27-3 m-benzylanisole 
• 1416981-82-2 2-benzyl-1,4-difluorobenzene 
• 1416981-83-3 1-benzyl-2-fluoro-4-methoxybenzene 

Relevant articles and documents

Palladium-Catalyzed Reductive Aminocarbonylation of Benzylammonium Triflates with o-Nitrobenzaldehydes for the Synthesis of 3-Arylquinolin-2(1 H)-ones

A palladium-catalyzed straightforward procedure for the synthesis of 3-arylquinolin-2(1H)-ones has been developed. The synthesis proceeds through a palladium-catalyzed reductive aminocarbonylation reaction of benzylic ammonium triflates with o-nitrobenzaldehydes, and a wide range of 3-arylquinolin-2(1H)-ones was obtained in moderate to good yields with very good functional group compatibility.

Synthesis of Dibenzylic Diselenides from Elemental Selenium and Benzylic Quaternary Ammonium Salts

Abstract: Substituted dibenzyl diselenides are synthesized in good yields (74–91 %) by SN2 nucleophilic substitution of benzylic trimethylammonium salts and diselenide dianion (Se2?), in situ generated from elemental selenium, under

Cu2O-catalyzed C–S coupling of quaternary ammonium salts and sodium alkane-/arene-sulfinates

A new protocol for the synthesis of (enantioenriched) benzylic sulfones via the Cu2O-catalyzed C–S bond cross coupling of alkane-/arene-sulfinates and (enantioenriched) benzylic quaternary ammonium salts has been developed. The product benzylic sulfones were obtained in good to high yields (75–96%). Chiral arylmethyl sulfones with high enantiomeric excess (90–94% ee) were also synthesized in the presence of Cu2O and 1,1′-bis-(diphenylphosphino)ferrocene (dppf).