129895-96-1

Basic information

• Product Name: C₆₀H₇₃N₅O₁₄
• CAS NO: 129895-96-1
• Molecular Weight: 1088.26
• Mol File: 129895-96-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₆₀H₇₃N₅O₁₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₆₀H₇₃N₅O₁₄(129895-96-1)
• EPA Substance Registry System: C₆₀H₇₃N₅O₁₄(129895-96-1)

Safety Data

• Hazardous Substances Data: 129895-96-1(Hazardous Substances Data)

Upstream product

• 144609-65-4 (+)-(9R,2S,2'S)-3-thioxo-9-(methoxycarbonyl)-2-(2'-ethyl-2',3'dihydroxypropyl)hexahydroindolizino<8,7-b>indole cyclohexylidene ketal 
• 144609-71-2 (R)-2-[((R)-2-Ethyl-1,4-dioxa-spiro[4.5]dec-2-yl)-(toluene-4-sulfonyloxy)-methyl]-3-thioxo-2,3,6,11-tetrahydro-1H,5H-indolizino[8,7-b]indole-11b-carboxylic acid methyl ester 
• 141521-23-5 (+)-(9R,2'S)-3-thioxo-9-(methoxycarbonyl)-2-(2'-ethyl-2',3'dihydroxypropyl)hexahydro-1-hydroxyindolizino<8,7-b>indole cyclohexylidene ketal 
• 141521-24-6 (+)-(9R,2'S)-3-thioxo-9-(methoxycarbonyl)-2-(2'-ethyl-2',3'dihydroxypropenyl)hexahydroindolizino<8,7-b>indole cyclohexylidene ketal 
• 141521-25-7 (R)-2-[1-((S)-2-Ethyl-1,4-dioxa-spiro[4.5]dec-2-yl)-meth-(Z)-ylidene]-2,3,6,11-tetrahydro-1H,5H-indolizino[8,7-b]indole-11b-carboxylic acid methyl ester 
• 141521-21-3 (R)-2-Ethyl-2-phenylsulfanylmethyl-1,4-dioxa-spiro[4.5]decane 
• 141521-22-4 (R)-2-Ethyl-1,4-dioxa-spiro[4.5]decane-2-carbaldehyde 
• 141521-20-2 (R)-(-)-2-ethyl-1-(phenylthio)-2,3-propanediol 
• 121464-71-9 (R)-(2-ethoxyoxiran-2-yl)methanol 
• 931-57-7 1-methoxy-cyclohex-1-ene 
• 4435-54-5 2-Methylene-1-butanol 
• 129895-92-7 (-)-(9R,2S,2'S)-3H-9-(methoxycarbonyl)-2-(2'-ethyl-2',3'dihydroxypropyl)hexahydroindolizino<8,7-b>indole cyclohexylidene ketal 
• 2182-14-1 vindoline 
• 4457-32-3 4-nitrobenzyl chloroformate 

Relevant articles and documents

Nonoxidative coupling methodology for the synthesis of the antitumor bisindole alkaloid vinblastine and a lower-half analogue: Solvent effect on the stereochemistry of the crucial C-15/C-18′ bond

The overall strategy for the synthesis of vinblastine (1) is based upon the nonoxidative cleavage of the tertiary amine (+)-18 to generate the intermediate delocalized cation 18a, which in the presence of an electron-rich aromatic nucleophile can be trapp