1290085-12-9

Basic information

• Product Name: (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(aminomethyl)-2-azabicyclo[2,2,1]heptane
• Synonyms: (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(aminomethyl)-2-azabicyclo[2,2,1]heptane
• CAS NO: 1290085-12-9
• Molecular Weight: 230.353
• Mol File: 1290085-12-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(aminomethyl)-2-azabicyclo[2,2,1]heptane(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(aminomethyl)-2-azabicyclo[2,2,1]heptane(1290085-12-9)
• EPA Substance Registry System: (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(aminomethyl)-2-azabicyclo[2,2,1]heptane(1290085-12-9)

Safety Data

• Hazardous Substances Data: 1290085-12-9(Hazardous Substances Data)

Upstream product

• 37662-06-9 ethyl <(S)-1-phenylethyl>iminoethanoate 
• 542-92-7 cyclopenta-1,3-diene 
• 215674-17-2 (1S,3R,4R)-2-[(S)-1-Phenylethylamino]-2-azabicyclo[2.2.1]heptane-3-carboxaldehyde 
• 215674-16-1 (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-hydroxymethyl-2-azabicyclo[2.2.1]heptane 
• 223473-32-3 (1S,3R,4R)-2-<(1S)-phenylethyl>-2-aza-bicyclo<2.2.1>heptane-3-carboxylic acid ethyl ester 
• 1290085-08-3 (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(azidomethyl)-2-azabicyclo[2,2,1]heptane 

Downstream Products

• 1290085-19-6 (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(N,N-dimethylaminomethyl)-2-azabicyclo[2,2,1]heptane 
• 1290085-14-1 (-)-(1S,3R,4R)-2-[(S)-1-phenylethyl]-3-(benzylaminomethyl)-2-azabicyclo[2.2.1]heptane 
• 1290085-15-2 (-)-(1S,3R,4R)-2-[(S)-1-phenylethyl]-3-{[(4-chlorophenyl)methylamino]methyl}-2-azabicyclo[2.2.1]heptane 
• 1290085-16-3 (-)-(1S,3R,4R)-2-[(S)-1-phenylethyl]-3-{[(4-fluorophenyl)methylamino]methyl}-2-azabicyclo[2.2.1]heptane 
• 1290085-17-4 (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-[(2-naphthylmethyl)aminomethyl]-2-azabicyclo[2,2,1]heptane 
• 1290085-18-5 (1S,3R,4R)-2-[(S)-1-phenylethyl]-3-[(9-anthrylmethyl)aminomethyl]-2-azabicyclo[2,2,1]heptane 

Relevant articles and documents

Application of polyamines and amino acid derivatives based on 2-azabicycloalkane backbone in enantioselective aldol reaction

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New 2-azanorbornyl derivatives: Chiral (N,N)-donating ligands for asymmetric catalysis

New chiral 2-azanorbornane derivatives were prepared and used as (N,N)-donating ligands in a copper-catalyzed Henry reaction yielding up to 62% ee.