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17,17-dimethyl-18-nor-5α-androst-13(14)-en-3-one is a synthetic anabolic steroid, which is a derivative of the naturally occurring hormone testosterone. 17,17-dimethyl-18-nor-5α-androst-13(14)-en-3-one is characterized by the presence of two methyl groups at the 17th carbon position and the absence of a carbon atom at the 18th position, which is referred to as "nor." The 5α configuration indicates the orientation of the hydroxyl group at the 5th carbon, and the 13(14)-en-3-one structure signifies a double bond between the 13th and 14th carbons, with a ketone group at the 3rd carbon. This steroid is known for its potent anabolic effects, which can promote muscle growth and strength, but it also has androgenic properties that can lead to masculinizing effects. It is important to note that the use of anabolic steroids outside of medical supervision can have serious health risks and is often prohibited in sports due to its potential to enhance performance unfairly.

1423-85-4

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1423-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1423-85:
(6*1)+(5*4)+(4*2)+(3*3)+(2*8)+(1*5)=64
64 % 10 = 4
So 1423-85-4 is a valid CAS Registry Number.

1423-85-4Downstream Products

1423-85-4Relevant academic research and scientific papers

Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17α-methyl steroids: synthesis and rearrangement

Bi, Honggang,Masse, Robert,Just, George

, p. 306 - 312 (1992)

A simple and convenient method has been developed to prepare sulfates of anabolic 17β-hydroxy-17α-methyl steroids.The sulfates of methandienone, 17α-methyltestosterone, mestanolone, oxandrolone, and stanozolol were prepared.Different A-ring functions were not affected under the sulfation condition.The buffered hydrolyses of these sulfates provided the 17-epimers of the original steroids and 17,17-dimethyl-18-nor-13(14)-ene steroids, presumably via the 17-carbocations. Keywords: steroids, tertiary sulfates; 17α-methyl steroids; 17β-methyl steroids; 17,17-dimethyl-18-norandrost-13(14)-enes; NMR

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