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23477-67-0

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23477-67-0 Usage

General Description

DL-Ethylgonendione is a synthetic hormone primarily used as an anabolic steroid in medical applications. It possesses a similar structure to naturally occurring hormones in the body, such as testosterone and estrogen. Due to its anabolic properties, it helps in promoting tissue building, and is commonly used for muscle growth and recovery. However, due to potential side effects and the risk of misuse, its usage is heavily regulated in many countries. Furthermore, DL-Ethylgonendione is also applied in scientific research, particularly in studies related to hormonal activities and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 23477-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,7 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23477-67:
(7*2)+(6*3)+(5*4)+(4*7)+(3*7)+(2*6)+(1*7)=120
120 % 10 = 0
So 23477-67-0 is a valid CAS Registry Number.

23477-67-0SDS

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 DL-Ethylgonendione

1.2 Other means of identification

Product number -
Other names 18-Methyl-4-oestren-3,17-dion

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:23477-67-0 SDS

23477-67-0Downstream Products

23477-67-0Relevant articles and documents

Synthesis of 13-alkyl-gon-4-ones

-

, (2008/06/13)

The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.

Steroid total synthesis. IX. Alternative routes to (+ -)- and (+)-estr-4-ene-3,17-dione and (+ -)-13 beta-13 -ethylgon-4-ene-3,17-dione via novel nitrile intermediates.

Cohen,Banner,Borer,Mueller,Yang,Rosenberger,Saucy

, p. 3385 - 3392 (2007/10/06)

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Steroid total synthesis. VII. ( )-Estr-4-ene-3, 17-dione and ( ) 13 -ethyl-gon-4-ene-3, 17-dione.

Rosenberger,Duggan,Saucy

, p. 1333 - 1339 (2007/10/11)

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