141294-37-3

Basic information

• Product Name: (R,R)-N-(1,2,2-trimethylpropyl)phenylethyl-1-amine α-methylbenzylamine
• Synonyms: (R,R)-N-(1,2,2-trimethylpropyl)phenylethyl-1-amine α-methylbenzylamine
• CAS NO: 141294-37-3
• Molecular Weight: 205.343
• Mol File: 141294-37-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (R,R)-N-(1,2,2-trimethylpropyl)phenylethyl-1-amine α-methylbenzylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (R,R)-N-(1,2,2-trimethylpropyl)phenylethyl-1-amine α-methylbenzylamine(141294-37-3)
• EPA Substance Registry System: (R,R)-N-(1,2,2-trimethylpropyl)phenylethyl-1-amine α-methylbenzylamine(141294-37-3)

Safety Data

• Hazardous Substances Data: 141294-37-3(Hazardous Substances Data)

Upstream product

• 31519-48-9 C₁₄H₂₁N 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 141393-92-2 (R)-α-methyl-N-(1,2,2-trimethylpropylidene)benzenemethanamine 
• 917-54-4 methyllithium 
• 254745-01-2 (R)-N-(2,2-dimethylpropylidene)-1-phenylethylamine 
• 31519-48-9 N-<3,3-Dimethyl-butyliden-(2)>-DL-α-phenyl-ethylamin 
• 630-19-3 pivalaldehyde 
• 75-97-8 3,3-dimethyl-butan-2-one 

Downstream Products

• 3850-30-4 (R)-1,2,2-trimethylpropylamine 
• 147852-31-1 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-N-((R)-1,2,2-trimethyl-propyl)-propionamide 
• 3907-04-8 Pinakolylamin-phthalsaeuremonoamid 

Relevant articles and documents

Step-efficient access to chiral primary amines

Routes to enantioenriched amines are outlined that employ reductive amination and carbanion addition methods. The strategies require either one or two reaction steps from prochiral carbonyl compounds for the synthesis of the corresponding chiral primary amines. Georg Thieme Verlag Stuttgart New York.

Asymmetric reductive amination: Convenient access to enantioenriched alkyl-alkyl or aryl-alkyl substituted α-chiral primary amines

A two-step procedure for producing optically active, high value primary amines has been developed. The first and key step is the asymmetric reductive amination of a prochiral alkyl alkyl (acyclic or cyclic) or aryl alkyl (acyclic or cyclic) ketone with (R

Asymmetric reduction of enantiopure imines with zinc borohydride: Stereoselective synthesis of chiral amines

The first application of zinc borohydride in the reduction of enantiopure imines for the stereoselective preparation of both the enantiomers of secondary amines is described. A possible explanation of the stereoselectivity and of the reaction mechanism is