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"3α,11β,17,21-Tetrahydroxy-5β-pregnan-20-one 21-Acetate" is a complex steroidal chemical compound derived from the pregnane family, characterized by the presence of four hydroxyl groups at the 3α, 11β, 17, and 21 positions, and an acetate group at the 21 position. 3α,11β,17,21-Tetrahydroxy-5β-pregnan-20-one 21-Acetate exhibits a unique molecular structure that is significant in the field of organic chemistry and pharmacology, particularly in the study of steroid hormones and their derivatives. It is synthesized through a series of chemical reactions and is often used in research to understand the structure-activity relationships of steroidal compounds. The acetate group at the 21 position plays a crucial role in modulating the biological activity and pharmacokinetics of the molecule, making it an important target for drug design and development in various therapeutic areas, including endocrinology and reproductive health.

4004-80-2

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4004-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4004-80-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,0 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4004-80:
(6*4)+(5*0)+(4*0)+(3*4)+(2*8)+(1*0)=52
52 % 10 = 2
So 4004-80-2 is a valid CAS Registry Number.

4004-80-2SDS

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 [2-oxo-2-[(3R,5R,8S,9S,10S,11S,13S,14S,17R)-3,11,17-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-yl]ethyl] acetate

1.2 Other means of identification

Product number -
Other names 3|A,11|A,17,21-tetrahydroxy-5|A-pregnan-20-one 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:4004-80-2 SDS

4004-80-2Relevant academic research and scientific papers

Potential corticoid metabolites: Chemical synthesis of 3- and 21-monosulfates and their double-conjugates of tetrahydrocorticosteroids in the 5 α- and 5 β-series

Okihara, Rika,Mitamura, Kuniko,Hasegawa, Maki,Mori, Megumi,Muto, Akina,Kakiyama, Genta,Ogawa, Shoujiro,Iida, Takashi,Shimada, Miki,Mano, Nariyasu,Ikegawa, Shigeo

experimental part, p. 344 - 353 (2011/02/22)

Here, we describe the chemical synthesis of the complete sets of 18 novel 3- and 21-monosulfates and their double-conjugated form of tetrahydrocortisol (THF), tetrahydro-11-deoxycortisol (THS), and tetrahydrocortisone (THE) in the 5 α- and 5 β-series. The principal reactions involved are: (1) selective protection of a specific hydroxy group in substrates; (2) catalytic hydrogenation at C-5 of Δ4-3-ketosteroids with 10% Pd(OH) 2/C to yield 3-oxo-5 β-steroids and reductive allomerization with 10% Pd/C to yield 3-oxo-5 α-isomers; (3) reduction of the resulting 3-oxo-5 β- and 3-oxo-5 α-steroids to the corresponding 3 α-hydroxy-compounds with Zn(BH4)2 and K-Selectride, respectively; and (4) sulfation of hydroxy groups at C-3 and/or C-21 in the tetrahydrocorticosteroid derivatives with sulfur trioxide-triethylamine complex.

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