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Estrone 3-cyclohexyl ether is a synthetic compound derived from estrone, a naturally occurring estrogen hormone. It is characterized by the presence of a cyclohexyl group attached to the 3-position of the estrone molecule, which modifies its chemical properties and biological activity. This modification can lead to changes in its solubility, stability, and potential therapeutic applications. The compound is of interest in pharmaceutical research due to its potential effects on the endocrine system and its use in the development of drugs targeting estrogen receptors. It is important to note that the safety, efficacy, and specific applications of estrone 3-cyclohexyl ether are subject to ongoing scientific investigation and must be evaluated within the context of rigorous clinical trials and studies.

1624-63-1

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1624-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1624-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1624-63:
(6*1)+(5*6)+(4*2)+(3*4)+(2*6)+(1*3)=71
71 % 10 = 1
So 1624-63-1 is a valid CAS Registry Number.

1624-63-1Downstream Products

1624-63-1Relevant academic research and scientific papers

Eco-friendly synthesis of 3-etherified estrones

Zheng, Dong-Qing,Jing, Yu,Zheng, Bing-Ying,Ye, Yun-Fei,Xu, Sheng,Tian, Wei-Sheng,Ma, Hai-Yan,Ding, Kai

, p. 2164 - 2169 (2016)

The conventional etherification uses toxic or hardly degradable alkylating agents. An eco-friendly tandem etherification/aromatization is presented to prepare estrone 3-secondary ethers from easily available dienone 1. Three marketed 3-etherified estrogen drugs were synthesized with the method from commercial available starting material.

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