828291-16-3

Basic information

• Product Name: Benzenemethanamine, alpha-methyl-N-(2-methylcyclohexylidene)-, (alphaR)- (9CI)
• Synonyms: Benzenemethanamine, alpha-methyl-N-(2-methylcyclohexylidene)-, (alphaR)- (9CI)
• CAS NO: 828291-16-3
• Molecular Formula: C₁₅H₂₁N
• Molecular Weight: 215.33394
• Product Categories: METHYL
• Mol File: 828291-16-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzenemethanamine, alpha-methyl-N-(2-methylcyclohexylidene)-, (alphaR)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, alpha-methyl-N-(2-methylcyclohexylidene)-, (alphaR)- (9CI)(828291-16-3)
• EPA Substance Registry System: Benzenemethanamine, alpha-methyl-N-(2-methylcyclohexylidene)-, (alphaR)- (9CI)(828291-16-3)

Safety Data

• Hazardous Substances Data: 828291-16-3(Hazardous Substances Data)

Upstream product

• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 583-60-8 2-Methylcyclohexanone 

Downstream Products

• 79265-63-7 ((1S,2R)-2-Methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine; hydrochloride 
• 79265-63-7 ((1S,2R)-2-Methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine; hydrochloride 
• 116837-34-4 (αR,1R,2S)-(+)-cis-2-Methyl-N-(1-phenylethyl)cyclohexanamin 
• 53068-89-6 (S)-3-(1-methyl-2-oxocyclohexyl)-propionic acid methyl ester 
• 1372790-21-0 ethyl (S)-5-(1-methyl-2-oxocyclohexyl)pent-2-ynoate 
• 184035-09-4 (1R,2S)-2-Methyl-1-((R)-1-phenyl-ethylamino)-cyclohexanecarboxylic acid amide 

Relevant articles and documents

THE ASYMMETRIC MICHAEL PROCESS INVOLVING CHIRAL IMINES: THE DIASTEREOFACIAL DIFFERENTIATION ASPECT

A mechanism for the diastereofacial differentiation in the title reaction is proposed on the basis of the variation of the chiral auxiliary amines and of the examination of the crystal structure of enamino-ester 15.

Intramolecular reductive ketone-alkynoate coupling reaction promoted by (η2-propene)titanium

Intramolecular reductive coupling of cycloalkanones tethered to alkynoates in the presence of (η2-propene)titanium was successfully performed to provide hydroxy-esters in a diastereoselective manner. Subsequent lactonization afforded angularly

Asymmetric strecker synthesis of the four α-quaternary 1-amino-2-methylcyclohexanecarboxylic acids

The synthesis of the four 1-amino-2-methylcyclohexanecarboxylic acids 13, 14, 15, and 16 from diastereomeric mixtures of the α-amino nitriles 1-4 by successive application of conc. H2SO4, Pd/C H2, and conc. HCl is describe