213176-46-6

Basic information

• Product Name: (S)-2-((S)-2-Benzyloxycarbonylamino-3-tert-butoxycarbonylamino-propionylamino)-3-hydroxy-propionic acid methyl ester
• Synonyms: (S)-2-((S)-2-Benzyloxycarbonylamino-3-tert-butoxycarbonylamino-propionylamino)-3-hydroxy-propionic acid methyl ester
• CAS NO: 213176-46-6
• Molecular Weight: 439.466
• Mol File: 213176-46-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-((S)-2-Benzyloxycarbonylamino-3-tert-butoxycarbonylamino-propionylamino)-3-hydroxy-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-((S)-2-Benzyloxycarbonylamino-3-tert-butoxycarbonylamino-propionylamino)-3-hydroxy-propionic acid methyl ester(213176-46-6)
• EPA Substance Registry System: (S)-2-((S)-2-Benzyloxycarbonylamino-3-tert-butoxycarbonylamino-propionylamino)-3-hydroxy-propionic acid methyl ester(213176-46-6)

Safety Data

• Hazardous Substances Data: 213176-46-6(Hazardous Substances Data)

Upstream product

• 5680-80-8 methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride 
• 16947-84-5 N-[(benzyloxy)carbonyl]-3-[(tert-butoxycarbonyl)amino]-L-alanine 

Downstream Products

• 213176-53-5 2-((S)-1-{[2-((S)-1-{[2-((S)-1-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-ethyl)-oxazole-4-carbonyl]-amino}-2-tert-butoxycarbonylamino-ethyl)-oxazole-4-carbonyl]-amino}-2-tert-butoxycarbonylamino-ethyl)-oxazole-4-carboxylic acid methyl ester 
• 213176-52-4 2-((S)-1-{[2-((S)-1-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-ethyl)-oxazole-4-carbonyl]-amino}-2-tert-butoxycarbonylamino-ethyl)-oxazole-4-carboxylic acid methyl ester 
• 213176-48-8 2-((S)-1-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-ethyl)-oxazole-4-carboxylic acid methyl ester 
• 213176-50-2 2-((S)-1-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-ethyl)-oxazole-4-carboxylic acid 
• 213176-47-7 (S)-2-((S)-1-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-ethyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 

Relevant articles and documents

Natural products analogs as Scaffolds for supramolecular and combinatorial chemistry

A new class of analogs of natural products useful for supramolecular and combinatorial chemistry is presented. Starting from the structure of natural dolastatins, we have designed and synthesized a series of amino acid-based unnatural rigid platforms having multiple functional groups pointing in the same direction. The stereochemistry of the final product is entirely determined by the chirality of the constituent amino acids.