1054734-45-0

Basic information

• Product Name: 5⁽²⁰⁾-deoxy-5⁽²⁰⁾-sulfanyl-7-deoxy-13-[[(4S,5R)-2-(4-methoxyphenyl)-3-(tert-butyloxycarbonyl)-4-phenyl-1,3-oxazolidin-5-yl]carbonyl]baccatin III
• Synonyms: 5⁽²⁰⁾-deoxy-5⁽²⁰⁾-sulfanyl-7-deoxy-13-[[(4S,5R)-2-(4-methoxyphenyl)-3-(tert-butyloxycarbonyl)-4-phenyl-1,3-oxazolidin-5-yl]carbonyl]baccatin III
• CAS NO: 1054734-45-0
• Molecular Weight: 968.132
• Mol File: 1054734-45-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5⁽²⁰⁾-deoxy-5⁽²⁰⁾-sulfanyl-7-deoxy-13-[[(4S,5R)-2-(4-methoxyphenyl)-3-(tert-butyloxycarbonyl)-4-phenyl-1,3-oxazolidin-5-yl]carbonyl]baccatin III(CAS DataBase Reference)
• NIST Chemistry Reference: 5⁽²⁰⁾-deoxy-5⁽²⁰⁾-sulfanyl-7-deoxy-13-[[(4S,5R)-2-(4-methoxyphenyl)-3-(tert-butyloxycarbonyl)-4-phenyl-1,3-oxazolidin-5-yl]carbonyl]baccatin III(1054734-45-0)
• EPA Substance Registry System: 5⁽²⁰⁾-deoxy-5⁽²⁰⁾-sulfanyl-7-deoxy-13-[[(4S,5R)-2-(4-methoxyphenyl)-3-(tert-butyloxycarbonyl)-4-phenyl-1,3-oxazolidin-5-yl]carbonyl]baccatin III(1054734-45-0)

Safety Data

• Hazardous Substances Data: 1054734-45-0(Hazardous Substances Data)

Upstream product

• 358621-70-2 7-deoxy-5⁽²⁰⁾-deoxy-5⁽²⁰⁾-sulfanyl-13-oxobaccatin III 
• 358621-69-9 2-benzoyl-9-oxo-10-acetyl-4α(20)-epoxy-5-mesyltaxicine I 
• 1027565-02-1 1,2-O-benzylidene-9-oxo-10-acetyl-4α(20)-epoxy-5-mesyltaxicine I 
• 358621-75-7 1,2-O-benzylidene-9-oxo-10-acetyl-4α(20)-epoxytaxicine I 
• 155396-69-3 (2R,4S,5R)-(2R,4S,5R)-3-tert-butoxycarbonyl-2-(4-methoxyphenyl)-4-phenyl-1,3-oxazolidine-5-carboxylic acid 
• 358621-71-3 7-deoxy-5⁽²⁰⁾-deoxy-5⁽²⁰⁾-sulfanylbaccatin III 

Relevant articles and documents

Semisynthesis of D-ring modified taxoids: Novel thia derivatives of docetaxel

Two novel 5(20)-thia analogues of docetaxel have been synthesized from 10-deacetylbaccatin III or taxine B and isotaxine B. The key step of these syntheses is the concomitant thietane ring formation and acetylation of the tertiary alcohol at C-4. Both compounds are less cytotoxic than docetaxel but have divergent activity on microtubule disassembly.