Cas 158660-67-4,10-deacetyl-7,10-bis<(2,2,2-trichloroethoxy)carbonyl>-2-(hexahydro)baccatin III

158660-67-4

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Basic information

Product Name: 10-deacetyl-7,10-bis<(2,2,2-trichloroethoxy)carbonyl>-2-(hexahydro)baccatin III
Synonyms: 10-deacetyl-7,10-bis<(2,2,2-trichloroethoxy)carbonyl>-2-(hexahydro)baccatin III
CAS NO:158660-67-4
Molecular Formula:
Molecular Weight: 901.444
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 10-deacetyl-7,10-bis<(2,2,2-trichloroethoxy)carbonyl>-2-(hexahydro)baccatin III(CAS DataBase Reference)
NIST Chemistry Reference: 10-deacetyl-7,10-bis<(2,2,2-trichloroethoxy)carbonyl>-2-(hexahydro)baccatin III(158660-67-4)
EPA Substance Registry System: 10-deacetyl-7,10-bis<(2,2,2-trichloroethoxy)carbonyl>-2-(hexahydro)baccatin III(158660-67-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 158660-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 158660-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,6,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 158660-67:
(8*1)+(7*5)+(6*8)+(5*6)+(4*6)+(3*0)+(2*6)+(1*7)=164
164 % 10 = 4
So 158660-67-4 is a valid CAS Registry Number.

158660-67-4Upstream product

158660-67-4Downstream Products

158660-67-4Relevant academic research and scientific papers

Synthesis and Structure - Activity Relationships of New Antitumor Taxoids. Effects of Cyclohexyl Substitution at the C-3'-and/or C-2 of Taxotere (Docetaxel)

Ojima, Iwao,Duclos, Olivier,Zucco, Martine,Bissery, Marie-Christine,Combeau, C.,et al.

, p. 2602 - 2608 (2007/10/02)

Synthesis and cytotoxicity of the new analogs (11-13) of docetaxel possessing cyclohexyl groups instead of phenyl groups at the C-3' and/or C-2 benzoate positions are described. The C-2 cyclohexanecarboxylate analog of paclitaxel (15) is also synthesized

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