133961-99-6

Basic information

• Product Name: Benzenemethanol, 4-bromo-a-[[methyl(phenylmethyl)amino]methyl]-
• CAS NO: 133961-99-6
• Molecular Formula: C16H18BrNO
• Molecular Weight: 320.229
• Mol File: 133961-99-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 4-bromo-a-[[methyl(phenylmethyl)amino]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 4-bromo-a-[[methyl(phenylmethyl)amino]methyl]-(133961-99-6)
• EPA Substance Registry System: Benzenemethanol, 4-bromo-a-[[methyl(phenylmethyl)amino]methyl]-(133961-99-6)

Safety Data

• Hazardous Substances Data: 133961-99-6(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 1431664-66-2 C₁₀H₁₂BrNO 
• 99-73-0 para-bromophenacyl bromide 
• 103-67-3 benzyl-methyl-amine 
• 6291-68-5 2-(benzyl(methyl)amino)-1-(4'-bromophenyl)ethanone hydrochloride 
• 32017-76-8 (+/-)-2-(4-bromophenyl)oxirane 
• 131326-98-2 2-(benzyl-methyl-amino)-1-(4-bromo-phenyl)-ethanone 

Downstream Products

• 158587-31-6 (+/-)-(4RS)-4-(4-bromophenyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Method for Ir/f-amphox high-efficiency synthesis of chiral α- C-amino alcohol by virtue of catalytic oxidation 1,2- of P-aminoketone by using one-aminoketone

The invention discloses a method for efficiently synthesizing chiral 1,2-amino alcohol by catalyzing alpha-aminoketone through Ir/f-amphox. A ligand f-amphox used by the method can be more easily synthesized; the reaction has the characteristics of enanti

Synthesis, antiulcer and antidepressive activity of 4-(4-halophenyl)-2-phenyl-1,2,3,4-tetrahydroisoquinolines

4-(4-halophenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinolines 2a-c have been synthesized by two methods and their biochemical and pharmacological properties have been studied. Biochemical investigations showed that all the compounds are strong inhibitors of