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3-Methoxy-1-methylestra-1,3,5(10)-trien-17-one is a synthetic steroid compound with the chemical formula C20H26O2. It belongs to the family of estrane steroids and is a derivative of the natural hormone estrone. 3-Methoxy-1-methylestra-1,3,5(10)-trien-17-one has a unique chemical structure that includes a methoxy group and a methyl group attached to an estratriene backbone, which may confer specific properties and potential biological activities. Further research is necessary to fully elucidate the pharmacological and physiological effects of 3-Methoxy-1-methylestra-1,3,5(10)-trien-17-one.

2684-40-4

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2684-40-4 Usage

Uses

Used in Pharmaceutical Research:
3-Methoxy-1-methylestra-1,3,5(10)-trien-17-one is utilized as a research compound for the development of hormone-based medications. Its unique structure and potential biological activities make it a promising candidate for pharmaceutical applications.
Used in Hormone-Based Medications:
In the pharmaceutical industry, 3-Methoxy-1-methylestra-1,3,5(10)-trien-17-one is used as a key component in the formulation of hormone-based medications. Its estrane steroidal nature and derivative status from estrone suggest potential therapeutic uses related to hormonal balance and treatment of related conditions.
Further research is required to explore the full range of applications and to understand the safety and efficacy of 3-Methoxy-1-methylestra-1,3,5(10)-trien-17-one in various medical contexts.

Check Digit Verification of cas no

The CAS Registry Mumber 2684-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2684-40:
(6*2)+(5*6)+(4*8)+(3*4)+(2*4)+(1*0)=94
94 % 10 = 4
So 2684-40-4 is a valid CAS Registry Number.

2684-40-4Downstream Products

2684-40-4Relevant academic research and scientific papers

A (2)H N.M.R. study of the Steroidal Dienone-Phenol Rearrangement

Avent, Antony G.,Hanson, James R.,Yang-zhi, Ling,Sadler, Ian H.

, p. 2129 - 2132 (2007/10/02)

The extent of deuteriation is reported for the products of the dienone-phenol rearrangement of androsta-1,4-dien-3-ones using as catalysts (i) deuteriated acetic anhydride, acetic acid, and zinc chloride; (ii) deuterium bromide; and (iii) methanol, ethyl orthoformate, and sulphuric acid.The stereochemistry of the acid-catalysed enolization of 1-dehydrotestosterone is also reported.

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