103382-80-5

Basic information

• Product Name: (R)-C₅H₄NCH₂NHCH(Me)Cy
• CAS NO: 103382-80-5
• Molecular Weight: 218.342
• Mol File: 103382-80-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-C₅H₄NCH₂NHCH(Me)Cy(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-C₅H₄NCH₂NHCH(Me)Cy(103382-80-5)
• EPA Substance Registry System: (R)-C₅H₄NCH₂NHCH(Me)Cy(103382-80-5)

Safety Data

• Hazardous Substances Data: 103382-80-5(Hazardous Substances Data)

Upstream product

• 17430-98-7 [(1S)-1-cyclohexylethyl]amine 
• 6959-47-3 2-chloromethylpyridine hydrochloride 
• 1121-60-4 pyridine-2-carbaldehyde 

Downstream Products

• 1046476-58-7 [RuCl(CH₃C₆H₄CH(CH₃)2)(C₆H₁₁CH(CH₃)NHCH₂C₅H₄N)]⁽¹⁺⁾*SbF₆^(1-)=[RuCl(CH₃C₆H₄CH(CH₃)2)(C₆H₁₁CH(CH₃)NHCH₂C₅H₄N)]SbF₆ 

Relevant articles and documents

Asymmetric Catalysis, Part 91: Enantioselective Monophenylation of cis-1,2-Cyclopentanediol with Triphenylbismuth Diacetate and Chiral Copper(II) Complexes as Catalysts

The monophenylation of cis-1,2-cyclopentanediol with triphenylbismuth diacetate in the presence of chiral Cu(II) complexes as catalysts gave cis-2-hydroxy-1-phenoxy-cyclopentane with enantiomeric excesses up to 38percent.The optically active ligands used were triamine derivatives of 2,6-bis(aminomethyl)pyridine and diamine derivatives of 2-(aminomethyl)pyridine.Selectivity in the monophenylation occurred only in the presence of the latter as auxiliary ligands. - Keywords.Enantioselective catalysis; Chiral Cu(II) complexes; Monophenylation; Triphenylbismuth diacetate; cis-1,2-Cyclopentanediol.