194864-02-3

Basic information

• Product Name: C-7,C-10-dibenzyloxycarbonyl-10-deacetyl baccatin III
• Synonyms: C-7,C-10-dibenzyloxycarbonyl-10-deacetyl baccatin III
• CAS NO: 194864-02-3
• Molecular Weight: 812.868
• Mol File: 194864-02-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: C-7,C-10-dibenzyloxycarbonyl-10-deacetyl baccatin III(CAS DataBase Reference)
• NIST Chemistry Reference: C-7,C-10-dibenzyloxycarbonyl-10-deacetyl baccatin III(194864-02-3)
• EPA Substance Registry System: C-7,C-10-dibenzyloxycarbonyl-10-deacetyl baccatin III(194864-02-3)

Safety Data

• Hazardous Substances Data: 194864-02-3(Hazardous Substances Data)

Upstream product

• 32981-86-5 10-deacetylbaccatin III 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 849213-19-0 C₆₅H₇₇NO₁₉ 
• 849213-15-6 TPI₂₈₇ 
• 849213-17-8 C₄₆H₆₃NO₁₅ 
• 849213-25-8 9-α-hydroxy-10-α-acetyl-2'(R,S)-hydroxy-3'(S)-isobutyl-3'-(N-t-butoxycarbonyl)-taxane 
• 849213-26-9 TPI 287 
• 942950-93-8 C₄₆H₆₃NO₁₅ 
• 1051405-83-4 C₄₃H₆₁NO₁₅ 
• 849213-24-7 C₅₅H₈₉NO₁₅Si₂ 
• 849213-23-6 C₅₃H₈₇NO₁₄Si₂ 
• 849213-21-4 C₅₃H₈₅NO₁₄Si₂ 
• 849213-22-5 C₅₃H₈₃NO₁₄Si₂ 
• 849213-20-3 C₄₁H₅₇NO₁₄ 
• 849213-14-5 C₄₃H₆₁NO₁₅ 
• 942485-81-6 C₅₅H₈₉NO₁₅Si₂ 

Relevant articles and documents

A Mild and Convenient Semi-Synthesis of Docetaxel from 10-Deacetyl Baccatin III

A novel protocol for the semi-synthesis of docetaxel was achieved in four steps from 10-deacetyl baccatin III with an overall yield of 50%. The key step is the selective protection of the C(7) and C(10) hydroxyl groups of 10-deacetyl baccatin III, utilizi

TAXANE AND ABEO-TAXANE ANALOGS

The present application discloses new taxane analogs, intermediates and methods for producing them. The present application is also directed to pharmaceutical formulations comprising abeo-taxanes and methods of treating cancer with the abeo-taxanes.

TAXANE ANALOGS FOR THE TREATMENT OF BRAIN CANCER

Provided herein are compounds and methods for the treatment of brain cancer in a mammal, wherein the method comprises the administration to the mammal a compound that stabilizes tubulin dimers or microtubles at G2-M interface during mitosis but is not a s