176908-55-7

Basic information

• Product Name: (S)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid methyl ester
• Synonyms: (S)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid methyl ester
• CAS NO: 176908-55-7
• Molecular Weight: 533.665
• Mol File: 176908-55-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid methyl ester(176908-55-7)
• EPA Substance Registry System: (S)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid methyl ester(176908-55-7)

Safety Data

• Hazardous Substances Data: 176908-55-7(Hazardous Substances Data)

Upstream product

• 4152-79-8 1,2-O-isopropylidene-5-methyl-5-deoxy-α-D-xylofuranose 
• 197567-43-4 Dithiocarbonic acid S-methyl ester O-((3aR,5R,6R,6aR)-2,2,5,6-tetramethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl) ester 
• 176908-52-4 2,4-di-O-benzyl-3,5-dideoxy-3-methyl-D-ribose diethyl dithioacetal 
• 176908-53-5 (2R,3R,4R)-2,4-Bis-benzyloxy-3-methyl-pentanal 
• 176908-50-2 5-deoxy-1,2-O-isopropylidene-3-methene-α-D-xylose 
• 176908-51-3 3,5-dideoxy-3-methyl-D-ribose diethyl dithioacetal 
• 37105-85-4 (3aR,5R,6R,6aR)-2,2,5,6-tetramethyl-tetrahydrofuro[2,3-d][1,3]dioxole 
• 32453-67-1 5-deoxy-1,2-O-isopropylidene-α-D-erythro-pentofuranos-3-ulose 
• 83537-82-0 (S)-O-benzyl-α-methylserine methyl ester 
• 176908-54-6 2,4-di-O-benzyl-3,5-dideoxy-3-methyl-D-ribonic acid 
• 104467-82-5 5-deoxy-1,2-O-ispropylidene-3=C-methyl-α-D-ribofuranose 

Downstream Products

• 176908-56-8 (S)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid 

Relevant articles and documents

Synthesis of conagenin analogs modified at 3'-carbon atom

Three conagenin analogs modified at 3'-carbon centre and their diastereoisomers at position C-2 mere synthesized. The synthesis of the acylating carboxylic acids 13, 22 and 33 having stereotriads were elaborated starling from D-xylose performing stereoselective reactions.