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10-Oxo Docetaxel, also known as Docetaxel EP Impurity B, is a novel taxoid with significant anti-tumor properties. It serves as an intermediate in the synthesis of Docetaxel (D494420), a widely used chemotherapy drug. As a pale yellow solid, 10-Oxo Docetaxel exhibits unique chemical properties, including instability in solution and a tendency to epimerize.

167074-97-7

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167074-97-7 Usage

Uses

Used in Pharmaceutical Industry:
10-Oxo Docetaxel is used as an intermediate in the synthesis of Docetaxel for its remarkable anti-tumor properties. It plays a crucial role in the development of cancer treatment drugs, particularly for the production of Docetaxel, which is effective against various types of cancer.
Used in Cancer Treatment:
10-Oxo Docetaxel is used as a precursor in the production of Docetaxel, a potent chemotherapeutic agent. It contributes to the development of cancer-fighting drugs that can be used to treat a wide range of malignancies, including breast, lung, gastric, and prostate cancers, among others.
Used in Research and Development:
10-Oxo Docetaxel is utilized in research and development for the study of taxoid compounds and their potential applications in cancer therapy. Its unique chemical properties and anti-tumor effects make it a valuable subject for scientific investigation and the development of new cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 167074-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,0,7 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167074-97:
(8*1)+(7*6)+(6*7)+(5*0)+(4*7)+(3*4)+(2*9)+(1*7)=157
157 % 10 = 7
So 167074-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C43H51NO14/c1-22-26(55-37(51)32(48)30(24-15-11-9-12-16-24)44-38(52)58-39(3,4)5)20-43(53)35(56-36(50)25-17-13-10-14-18-25)33-41(8,34(49)31(47)29(22)40(43,6)7)27(46)19-28-42(33,21-54-28)57-23(2)45/h9-18,26-28,30,32-33,35,46,48,53H,19-21H2,1-8H3,(H,44,52)/t26?,27-,28+,30-,32?,33-,35?,41+,42-,43+/m0/s1

167074-97-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-Oxo Docetaxel

1.2 Other means of identification

Product number -
Other names (|AR,|AS)-|A-[[(1,1-Dimethylethoxy)carbonyl]amino]-|A-hydroxybenzenepropanoic Acid (2aR,4S,4aS,9S,11S,12S,12aR,12bS)-12b-(Acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5,6-dioxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl Ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:167074-97-7 SDS

167074-97-7Upstream product

167074-97-7Downstream Products

167074-97-7Relevant articles and documents

Preparation method 10 - carbonyl docetaxel

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Paragraph 0029-0042; 0048-0049, (2021/11/06)

The invention discloses a preparation method of 10 - carbonyl docetaxel, and the technical scheme of the invention comprises the following steps: S1: dissolving docetaxel solvent, adding heavy metal salt, stirring and reacting, carrying out suction filtra

PHARMACEUTICAL COMPOSITION CONTAINING A TAXANE DERIVATIVE, DESTINED FOR THE PREPARATION OF AN INFUSION SOLUTION, METHOD OF PREPARATION THEREOF AND USE THEREOF

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Page/Page column 18-23, (2008/06/13)

A pharmaceutical composition containing a taxane derivative, destined for the preparation of an infusion solution for administration to patients, containing a concentrate consisting of a pharmaceutically effective amount of docetaxel, a suitable solvent,

Synthesis and evaluation of C-seco paclitaxel analogues

Appendino, Giovanni,Danieli, Bruno,Jakupovic, Jasmin,Belloro, Emanuela,Scambia, Giovanni,Bombardelli, Ezio

, p. 4273 - 4276 (2007/10/03)

Starting from 7,9diTes-10-dehydro C-secobaccatin III (4a), C-seco analogues of paclitaxel retaining biological activity were synthesised.

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