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64313-94-6

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64313-94-6 Usage

Chemical Properties

White Solid

Uses

Cortisol derivatiove. Shows binding affinities for the cytosol glucocorticoid receptor.

Check Digit Verification of cas no

The CAS Registry Mumber 64313-94-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64313-94:
(7*6)+(6*4)+(5*3)+(4*1)+(3*3)+(2*9)+(1*4)=116
116 % 10 = 6
So 64313-94-6 is a valid CAS Registry Number.

64313-94-6SDS

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 21-acetoxy-11β,17α-dihydroxy-5β-pregnane-3,20-dione

1.2 Other means of identification

Product number -
Other names RU 18760

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:64313-94-6 SDS

64313-94-6Relevant articles and documents

Spectroscopic evaluation of synthesized 5β-dihydrocortisol and 5β-dihydrocortisol acetate binding mechanism with human serum albumin and their role in anticancer activity

Kallubai, Monika,Reddy, Srinivasa P.,Dubey, Shreya,Ramachary, Dhevalapally B.,Subramanyam, Rajagopal

, p. 1 - 18 (2018/02/22)

Our study focus on the biological importance of synthesized 5β-dihydrocortisol (Dhc) and 5β-dihydrocortisol acetate (DhcA) molecules, the cytotoxic study was performed on breast cancer cell line (MCF-7) normal human embryonic kidney cell line (HEK293), th

Direct organocatalytic stereoselective transfer hydrogenation of conjugated olefins of steroids

Ramachary, Dhevalapally B.,Sakthidevi, Rajasekar,Reddy, P. Srinivasa

, p. 13497 - 13506 (2013/09/02)

Kinetically controlled and organocatalytic syn-selective transfer hydrogenation has been successfully demonstrated for the reduction of the enone functional group of various steroids. Herein, diastereoselective synthesis of many 5β-steroids have been reported through organocatalysis, which have broad medicinal and pharmaceutical applications. The mechanistic studies and the selectivity of the products clearly indicated that the catalyst 1b·d-CSA is mild enough to activate the various chiral cyclic enones through iminium ion formation during the organocatalytic transfer hydrogenations with Hantzsch ester 2a as a hydrogen source. Further, clear evidence for the selective formation of intermediate iminium species [I]+ have been characterized through on-line monitoring of controlled experiments by NMR and ESI-HRMS analyses.

Chemical conversion of corticosteroids to 3α,5α-tetrahydro derivatives. Synthesis of allotetrahydrocortisol glucuronides and allotetrahydrocortisone glucuronides

Hosoda,Osanai,Fukasawa,Nambara

, p. 1949 - 1952 (2007/10/02)

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