352695-16-0

Basic information

• Product Name: (1R_.E)-N-(2-methylcyclohexylidene)-1-phenylethanamine
• Synonyms: (1R_.E)-N-(2-methylcyclohexylidene)-1-phenylethanamine
• CAS NO: 352695-16-0
• Molecular Weight: 215.338
• Mol File: 352695-16-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (1R_.E)-N-(2-methylcyclohexylidene)-1-phenylethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1R_.E)-N-(2-methylcyclohexylidene)-1-phenylethanamine(352695-16-0)
• EPA Substance Registry System: (1R_.E)-N-(2-methylcyclohexylidene)-1-phenylethanamine(352695-16-0)

Safety Data

• Hazardous Substances Data: 352695-16-0(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 161151-77-5 *,S^*)>-α-(acetyloxy)-1-methyl-2-oxocyclohexanepropanoic acid methyl ester 
• 441350-32-9 (S)-3-{(S)-1-Methyl-2-[(E)-(R)-1-phenyl-ethylimino]-cyclohexyl}-butyric acid methyl ester 
• 118664-19-0 (4R,4aS)-4,4a-Dimethyl-1-((R)-1-phenyl-ethyl)-3,4,4a,5,6,7-hexahydro-1H-quinolin-2-one 
• 63975-59-7 (R)-(-)-4a-methyl-4,4a,5,6,7,8-hexahydro-3H-naphthalene-2-one 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 91306-30-8 (R)-(+)-2-methyl-2-(3-oxobutyl)cyclohexanone 
• 125446-66-4 (S)-2-methyl-2-(3-oxopentyl)cyclohexanone 
• 3203-30-3 (2S,4aS)-1,1,4a-trimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-ol 
• 58193-60-5 (S)-1,1,4a-trimethyl-3,4,4a,5,6,7-hexahydronaphthalen-2(1H)-one 
• 787610-05-3 2-(Diethoxy-phosphoryl)-3-((S)-1-methyl-2-oxo-cyclohexyl)-propionic acid 
• 67301-13-7 (Z)-1-methyl-2-oxocyclohexane-2-propenoic acid methyl ester 
• 67301-11-5 (E)-1-methyl-2-oxocyclohexane-2-propenoic acid methyl ester 
• 98-86-2 acetophenone 
• 53068-89-6 (R)-(+)-2-(2'-carbomethoxyethyl)-2-methylcyclohexanone 

Relevant articles and documents

Enantioselective Synthesis of Quaternary Carbon Centers trough Michael-Type Alkylation of Chiral Imines

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INDOLE CARBOXAMIDE DERIVATIVES AND USES THEREOF

A compound of Formula (I) is provided that has been shown to be useful for treating a disease, disorder or syndrome that is mediated by the transportation of essential molecules in the mmpL3 pathway: (I) wherein R1, R2, R3, R4, R5 and R6 are as defined herein.

High pressure activation in the asymmetric Michael addition of chiral imines to alkyl and aryl crotonates

High pressure-mediated Michael addition of chiral imines derived from 2-methylcyclopentanone, 2-methylcyclohexanone and optically active 1-phenylethylamine, to methyl and phenyl crotonates was investigated. The corresponding adducts were obtained in fair yields and with a high degree of regio-, diastereo- and enantioselectivity.