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9,11-Dehydrodeoxycorticosterone 21-acetate is a chemical compound derived from deoxycorticosterone, a hormone produced by the adrenal glands. It is characterized by the removal of two hydrogen atoms from the 9 and 11 positions, which results in the formation of a double bond, and the acetylation of the 21st carbon atom. This modification can alter the compound's biological activity and properties. In the context of pharmaceuticals or chemical research, such alterations are often explored to understand the structure-activity relationships of hormones and to develop potential therapeutic agents. The compound may be used in scientific studies to investigate the effects of structural changes on hormone function and to potentially create new drugs with specific therapeutic benefits.

4780-55-6

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4780-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4780-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,8 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4780-55:
(6*4)+(5*7)+(4*8)+(3*0)+(2*5)+(1*5)=106
106 % 10 = 6
So 4780-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C23H30O4/c1-14(24)27-13-21(26)20-7-6-18-17-5-4-15-12-16(25)8-10-22(15,2)19(17)9-11-23(18,20)3/h9,12,17-18,20H,4-8,10-11,13H2,1-3H3/t17-,18-,20+,22-,23-/m0/s1

4780-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(8S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

1.2 Other means of identification

Product number -
Other names 9,11-Dehydrodeoxycorticosterone 21-acetate

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:4780-55-6 SDS

4780-55-6Downstream Products

4780-55-6Relevant academic research and scientific papers

New Synthesis of the Corticosterone Side-Chain

Solyom, Sandor,Szilagyi, Katalin,Toldy, Lajos

, p. 153 - 160 (2007/10/02)

Condensation reactions between azlactone 2 and 17-ketosteroids 1 followed by opening of the azlactone ring with sodium methanolate yields methyl 20-benzoylamino-17(20)-pregnen-21-oates 6.Reduction of the ester and subsequent hydrolysis produce compounds with the corticosterone side-chain as well as a ring-closed product of new type.

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