158045-02-4

Basic information

• Product Name: (R)-3-amino-2-benzylpropane
• Synonyms: (R)-3-amino-2-benzylpropane
• CAS NO: 158045-02-4
• Molecular Weight: 165.235
• Mol File: 158045-02-4.mol

Chemical Properties

• CAS DataBase Reference: (R)-3-amino-2-benzylpropane(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-amino-2-benzylpropane(158045-02-4)
• EPA Substance Registry System: (R)-3-amino-2-benzylpropane(158045-02-4)

Safety Data

• Hazardous Substances Data: 158045-02-4(Hazardous Substances Data)

Upstream product

• 129600-11-9 (S)-1-acetoxy-2-benzyl-3-(methanesulfonyloxy)propane 
• 254990-76-6 (R)-1-acetoxy-3-azido-2-benzylpropane 
• 110270-49-0 (R)-3-acetoxy-2-benzyl-1-propanol 
• 2612-30-8 2-benzyl-1,3-propanediol 
• 173216-45-0 (R)-3-azido-2-benzylpropanol 

Downstream Products

• 254990-90-4 (R)-2-benzyl-[N-(benzyloxycarbonyl)glycyl]-[N'-(tert-butoxycarbonyl)-D-alanyl]-1,3-propanediamine 
• 254990-89-1 (R)-2-benzyl-[N-(benzyloxycarbonyl)glycyl]-[N'-(tert-butoxycarbonyl)-L-alanyl]-1,3-propanediamine 
• 254990-88-0 (S)-2-benzyl-[N-(benzyloxycarbonyl)]-[N'-(tert-butoxycarbonyl)-D-alanyl]-1,3-propanediamine 
• 254990-87-9 (S)-2-benzyl-[N-(benzyloxycarbonyl)]-[N'-(tert-butoxycarbonyl)-L-alanyl]-1,3-propanediamine 
• 254990-95-9 (R)-2-benzyl-[N-(benzyloxycarbonyl)]-[N'-(tert-butoxycarbonyl)]-1,3-propandiamine 
• 254990-85-7 (S)-(N-acetyl)-2-benzyl-[N-(benzyloxycarbonyl)]propandiamine 
• 254990-82-4 Methanesulfonic acid (R)-2-(benzyloxycarbonylamino-methyl)-3-phenyl-propyl ester 
• 254990-83-5 (R)-3-azido-2-benzyl-[N-(benzyloxycarbonyl)]propanamine 
• 254990-84-6 (S)-2-benzyl-[N-(benzyloxycarbonyl)]propandiamine 
• 254990-97-1 (R)-2-benzyl-3-[(tert-butoxycarbonyl)amino]propanol 
• 254990-98-2 (R)-3-azido-2-benzyl-3-[(tert-butoxycarbonyl)]propanamine 
• 254990-93-7 (R)-2-benzyl-[N-(tert-butoxycarbonyl)]-1,3-propandiamine 

Relevant articles and documents

Synthesis of asymmetrized 2-benzyl-1,3-diaminopropane by a chemoenzymatic route: A tool for combinatorially developing peptidomimetics

Both enantiomers of monoacetamide 5, together with 'dipeptides' 30a,b and monocarbamates 24, (R)-43 and (S)-43, all derived from 2-benzyl-1,3- diaminopropane 4, were synthesized by a chemoenzymatic route starting from the known monoacetate 12. The behaviour of 4 and of the bis(acylated) derivatives 8-11 with respect to hydrolytic enzymes is also presented, together with an extensive study on the configurational stability of monoacylated derivatives of 4.