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6β,19-Cycloandrost-4-ene-3,17-dione is a synthetic steroid with the molecular formula C19H26O2. It is a derivative of androst-4-ene-3,17-dione, which is a naturally occurring steroid hormone. 6β,19-Cycloandrost-4-ene-3,17-dione features a cycloalkane ring between the 6β and 19 positions, which is a structural modification that can alter its biological activity. It is used in scientific research to study the effects of steroidal compounds on various biological processes, such as hormone regulation and cellular metabolism. Due to its structural similarity to natural steroids, it can be used to understand the mechanisms of steroid action and to develop new therapeutic agents. The compound is typically synthesized in a laboratory setting and is not found naturally in the environment.

2352-95-6

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2352-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2352-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2352-95:
(6*2)+(5*3)+(4*5)+(3*2)+(2*9)+(1*5)=76
76 % 10 = 6
So 2352-95-6 is a valid CAS Registry Number.

2352-95-6Relevant academic research and scientific papers

6β,19-Bridged androstenedione analogs as aromatase inhibitors

Komatsu, Sachiko,Yaguchi, Ayaka,Yamashita, Kouwa,Nagaoka, Masao,Numazawa, Mitsuteru

, p. 884 - 889 (2009)

Inhibition of aromatase is an efficient approach for the prevention and treatment of breast cancer. New 6β,19-bridged steroid analogs of androstenedione, 6β,19-epithio- and 6β,19-methano compounds 11 and 17, were synthesized starting from 19-hydroxyandros

Some new reactions of poly(per)fluoroalkanesulfonyl fluorides with steroidal molecules

Tian, Wei-Sheng,Lei, Zhen,Chen, Ling,Huang, Ying

, p. 305 - 308 (2000)

The reactions of poly(per)fluoroalkanesulfonyl fluorides with steroidal ketones and alkenyl halides as well as 19-hydroxyl steroids were studied in detail. Utilizing these reactions, some steroidal molecules with the biological activity or structurally un

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