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methyl (3alpha,5beta)-3-hydroxy-12-oxochol-9(11)-en-24-oate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65065-56-7

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65065-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65065-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,6 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65065-56:
(7*6)+(6*5)+(5*0)+(4*6)+(3*5)+(2*5)+(1*6)=127
127 % 10 = 7
So 65065-56-7 is a valid CAS Registry Number.

65065-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (4R)-4-[(3R,5R,8S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-12-oxo-1,2,3,4,5,6,7,8,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]pentanoate

1.2 Other means of identification

Product number -
Other names 2-phenoxyethyl 4-(2,3-dimethoxyphenyl)-7-(4-methoxyphenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

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:65065-56-7 SDS

65065-56-7Relevant academic research and scientific papers

Synthesis and biological activity of novel deoxycholic acid derivatives

Popadyuk, Irina I.,Markov, Andrey V.,Salomatina, Oksana V.,Logashenko, Evgeniya B.,Shernyukov, Andrey V.,Zenkova, Marina A.,Salakhutdinov, Nariman F.

, p. 5022 - 5034 (2015/08/03)

We report the synthesis and biological activity of new semi-synthetic derivatives of naturally occurring deoxycholic acid (DCA) bearing 2-cyano-3-oxo-1-ene, 3-oxo-1(2)-ene or 3-oxo-4(5)-ene moieties in ring A and 12-oxo or 12-oxo-9(11)-ene moieties in ring C. Bioassays using murine macrophage-like cells and tumour cells show that the presence of the 9(11)-double bond associated with the increased polarity of ring A or with isoxazole ring joined to ring A, improves the ability of the compounds to inhibit cancer cell growth.

HYDROGENATION OF 12-OXO-5β-CHOL-9(11)-ENATES ON PLATINUM

Kasal, Alexander

, p. 1839 - 1849 (2007/10/02)

Methyl 12-oxo-5β-chol-9(11)-enates with various substituents in the position 3 were prepared and the conditions were found under which hydrogenation of the supposedly resistent double bond of 9α-cholanates takes place.Under these conditions the products of deoxygenation in the position 12, and in the case of the hydrogenation of 3-oxo derivatives the products of deoxygenation in the position 3, were isolated as side-products of this reaction.The rate of the last mentioned reaction is a function of the excess of the catalyst.

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