1101181-32-1

Basic information

• Product Name: C₄₂H₅₉N₅O₆S
• Synonyms: C₄₂H₅₉N₅O₆S
• CAS NO: 1101181-32-1
• Molecular Weight: 762.026
• Mol File: 1101181-32-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₄₂H₅₉N₅O₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₄₂H₅₉N₅O₆S(1101181-32-1)
• EPA Substance Registry System: C₄₂H₅₉N₅O₆S(1101181-32-1)

Safety Data

• Hazardous Substances Data: 1101181-32-1(Hazardous Substances Data)

Upstream product

• 921928-01-0 (R)-perfluorophenyl 1-methylpiperidine-2-carboxylate 
• 1101181-31-0 C₄₂H₅₇N₅O₆S 
• 368870-65-9 (2S,4R)-4-((tert-butoxycarbonyl)amino)-2-methyl-5-phenylpentanoic acid 
• 1467751-12-7 tert-butyl (3R,5R)-5-(tert-butyldimethylsilyloxy)-6-hydroxy-2-methylhexan-3-ylcarbamate 
• 156592-93-7 (3S)-4-<(tert-butyldimethylsilyl)oxy>-3-methylbutanol 
• 42406-72-4 L-isoleucine benzyl ester 
• 41447-17-0 (R)-1-methylpiperidine-2-carboxylic acid 
• 204917-42-0 (3S)-4-(tert-butyldimethylsilanyloxy)-3-methylbutyraldehyde 
• 862387-31-3 (S)-4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-butyric acid 
• 1017624-85-9 (R)-4-tert-butoxycarbonylamino-3-methyl-5-phenylpentanoic acid benzyl ester 
• 796039-47-9 (1R,3S)-(1-benzyl-4-hydroxy-3-methylbutyl)carbamic acid tert-butyl ester 

Downstream Products

• 1427513-79-8 C₃₇H₅₇N₅O₇S 

Relevant articles and documents

An enantioselective total synthesis of tubulysin V

Tubulysin V has been enantioselectively synthesized from the units of dipeptide 23, Tuv and Tup. The features of this synthetic strategy is included three portions, the Tuv fragment 17 was diastereoselectively synthesized from the D-malic acid, the stereocenters of the Tup unit was constructed by the asymmetric reduction as well as methylation, and the epimerization for several known methods was successfully avoided by condensation of fragment 19 with 24, and by deprotection with hydrogenation.