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34988-34-6

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  • N-[(3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ylidene)amino]-4-methyl-benzenesulfonamide

    Cas No: 34988-34-6

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  • N-[(3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ylidene)amino]-4-methyl-benzenesulfonamide cas 34988-34-6

    Cas No: 34988-34-6

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34988-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34988-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,8 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34988-34:
(7*3)+(6*4)+(5*9)+(4*8)+(3*8)+(2*3)+(1*4)=156
156 % 10 = 6
So 34988-34-6 is a valid CAS Registry Number.

34988-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(3-hydroxy-10,13-dimethyl-3,4,7,8,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)-ylidene)-4-methylbenzenesulfonohydrazide

1.2 Other means of identification

Product number -
Other names 5alpha-Spirost-9(11)-en-3beta-ol,(25R)

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:34988-34-6 SDS

34988-34-6Downstream Products

34988-34-6Relevant articles and documents

Synthesis of the anti-prostate cancer drug abiraterone acetate

Ma, Siyue,Li, Jianheng,Tang, Huayang,Xu, Feng

, p. 461 - 469 (2018/03/27)

Abiraterone acetate is used for the treatment of castration-resistant prostate cancer. Abiraterone acetate was synthesized from dehydroepiandrosterone via a three-step reaction including the formation of tosylhydrazone, cross-coupling reaction and acetylation, and a two-step purification including column chromatography and recrystallization with an overall yield of 51.9%. Here, an improved procedure for the preparation of abiraterone acetate is described. This synthetic process is of easy operation and low cost, which is suitable for industrialization.

SYNTHESIS OF ABIRATERONE AND RELATED COMPOUNDS

-

Paragraph 0201; 0202; 0203, (2014/02/15)

The present invention relates to processes for obtaining abiraterone and derivatives thereof, such as abiraterone acetate, by means of a Suzuki coupling through a steroid borate of general formula (IV) or a C—C coupling through a steroid hydrazone of general formula (II), as well as to intermediates useful in said processes.

Processes for the preparation of abiraterone and related compouds

-

Paragraph 0088; 0089; 0090, (2013/07/19)

The present invention relates to processes for obtaining abiraterone and derivatives thereof, such as abiraterone acetate, by means of a C-C coupling through a steroid hydrazone of general formula (II) or a Suzuki coupling through a steroid borate of general formula (IV), as well as to intermediates useful in said processes.

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