646026-96-2

Basic information

• Product Name: N-((S)-1-phenylethyl)octan-2-amine
• Synonyms: N-((S)-1-phenylethyl)octan-2-amine
• CAS NO: 646026-96-2
• Molecular Weight: 233.397
• Mol File: 646026-96-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-((S)-1-phenylethyl)octan-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-((S)-1-phenylethyl)octan-2-amine(646026-96-2)
• EPA Substance Registry System: N-((S)-1-phenylethyl)octan-2-amine(646026-96-2)

Safety Data

• Hazardous Substances Data: 646026-96-2(Hazardous Substances Data)

Upstream product

• 111-13-7 hexyl-methyl-ketone 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 629-05-0 n-octyne 
• 157646-18-9 (S)-(1-methylheptylidene)(1-phenylethyl)amine 

Downstream Products

• 34566-04-6 (S)-octan-2-amine 
• 693-16-3 (R)-2-octylamine 

Relevant articles and documents

Sequential reductive amination-hydrogenolysis: A one-pot synthesis of challenging chiral primary amines

Difficult-to-access chiral primary amines were formed in good to high yield and ee using a rare example of a one-pot synthesis from prochiral ketones (sequential reductive amination-hydrogenloysis). As a highlight we also demonstrate a one-pot reductive amination-hydrogenolysis-reductive amination (five reactions) of ortho-methoxyacetophenone resulting in the chiral diamine 1-(2-methoxyphenyl)ethyl-(2-pyridylmethyl)-amine (4) (58% overall yield, >99% ee), a new organocatalyst for aqueous enantioselective aldol reactions. Copyright

Aminoborohydrides. 6. Diastereoselective Reduction of the Carbon-Nitrogen Double Bond in Chiral Imines Using Lithium Diethylaminoborohydride and Lithium Diisopropylaminoborohydride.

Lithium aminoborohydrides (LAB), obtained by the reaction of n-BuLi with amine-boranes, readily reduce imines to the corresponding secondary amines.Lithium diethylaminoborohydride and lithium diisopropylaminoborohydride reduc