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(+/-)-Nortestosteron-acetat, also known as nortestosterone acetate, is a synthetic anabolic steroid derived from testosterone. It is a 19-nortestosterone (19-nor) steroid, which means it has a carbon atom missing at the 19th position in its structure, making it a potent androgen. This modification allows it to bypass certain metabolic pathways, resulting in a longer half-life and increased anabolic effects. Nortestosterone acetate is used in medical and veterinary applications, primarily for its muscle-building and performance-enhancing properties. It is also a precursor to other anabolic steroids, such as trenbolone and nandrolone. Due to its potent effects, nortestosterone acetate is subject to strict regulations and is often misused in sports for its performance-enhancing capabilities, leading to potential health risks and legal consequences.

5972-66-7

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5972-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5972-66-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,7 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5972-66:
(6*5)+(5*9)+(4*7)+(3*2)+(2*6)+(1*6)=127
127 % 10 = 7
So 5972-66-7 is a valid CAS Registry Number.

5972-66-7Upstream product

5972-66-7Downstream Products

5972-66-7Relevant academic research and scientific papers

Steroidal imidazole 1 carboxylic acid esters

Fahrenholtz,Boris,Kennedy Jr,Kierstead

, p. 337 - 342 (1974)

A variety of steroidal esters of imidazole 1 carboxylic acid and related acids was prepared by reaction of the steroidal alcohol with N,N' carbonyldiimidazole or by displacement of phenol from steroid phenylcarbonates. One compound, 21c (the imidazole 1 carboxylate of 19 norethisterone), was found to have an interesting separation of progestational from androgenic activity.

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.

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