155096-16-5

Basic information

• Product Name: (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester
• Synonyms: (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester
• CAS NO: 155096-16-5
• Molecular Weight: 455.551
• Mol File: 155096-16-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester(155096-16-5)
• EPA Substance Registry System: (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester(155096-16-5)

Safety Data

• Hazardous Substances Data: 155096-16-5(Hazardous Substances Data)

Upstream product

• 13734-41-3 t-Boc-L-valine 
• 7622-21-1 benzyl-(S)-(-)-2-hydroxy-3-phenylpropionate 

Downstream Products

• 155096-19-8 (S)-2-({(S)-2-[(2R,3R)-3-((2S,3S)-2-Benzyloxycarbonylamino-3-methyl-pentanoylamino)-2-methyl-butyryloxy]-3-methyl-butyryl}-methyl-amino)-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester 
• 155096-18-7 (S)-2-{[(S)-2-((2R,3R)-3-tert-Butoxycarbonylamino-2-methyl-butyryloxy)-3-methyl-butyryl]-methyl-amino}-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester 
• 155096-17-6 (S)-2-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-butyrylamino]-3-methyl-butyric acid (S)-1-benzyloxycarbonyl-2-phenyl-ethyl ester 

Relevant articles and documents

Isolation, Structure, and Synthesis of Dolastatin D, a Cytotoxic Cyclic Depsipeptide from the Sea Hare Dolabella auricularia

Dolastatin D (1), a cytotoxic cyclic depsipeptide possessing the novel β-amino acid (2R,3R)-3-amino-2-methylbutanoic acid as a component, has been isolated from the Japanese sea hare Dolabella auricularia.The absolute stereostructure of 1 was elucidated on the basis of spectroscopic analysis and chemical degradation and was further confirmed by synthesis.