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22798-98-7

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22798-98-7 Usage

General Description

Ecdysterone 2,3:20,22-diacetonide is a chemical compound derived from ecdysterone, a naturally occurring compound found in plants such as spinach and quinoa. It is a steroid hormone that is structurally similar to testosterone and is known for its potential anabolic effects, which can help to build muscle, increase strength, and improve athletic performance. Ecdysterone 2,3:20,22-diacetonide is often used as a supplement by bodybuilders and athletes to enhance their physical performance and recovery. Research suggests that it may also have potential health benefits, such as improving glucose metabolism, reducing inflammation, and protecting against oxidative stress. However, further studies are needed to fully understand its effects and safety profile.

Check Digit Verification of cas no

The CAS Registry Mumber 22798-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,9 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22798-98:
(7*2)+(6*2)+(5*7)+(4*9)+(3*8)+(2*9)+(1*8)=147
147 % 10 = 7
So 22798-98-7 is a valid CAS Registry Number.

22798-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 20-hydroxy-23,24-dinor-chol-4-en-3-one

1.2 Other means of identification

Product number -
Other names 20-hydroxy-20-methylpregn-4-en-3-one

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:22798-98-7 SDS

22798-98-7Relevant articles and documents

Synthesis of 20-Hydroxyecdysone Carboxylate Esters

Bobaev,Zavarzin,Blinnikov,Bobakulov, Kh. M.,Ramazanov, N. Sh.,Abdullaev

, p. 1088 - 1092 (2017/12/04)

Acylation of 20-hydroxy-2,3-O-isopropylideneecdysone (2) by carboxylic-acid anhydrides produced ecdysteroid derivatives containing various organic acids (5–12).

Selective Acetylation of 20-Hydroxyecdysone. Partial Synthesis of Some Minor Ecdysteroids and Analogues

Suksamrarn, Apichart,Pattanaprateep, Prasert

, p. 10633 - 10650 (2007/10/02)

Selective acetylation of the 2,3- and 20,22-acetonide and 2,3:20,22-diacetonide derivatives of 20-hydroxyecdysone and subsequent removal of the protecting groups led to partial synthesis of a number of mono-, di- and triacetate derivatives of 20-hydroxyecdysone.Some of these acetate derivatives are minor, naturally occurring ecdysteroids.

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