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3-Methoxy-18-methylestra-2,5(10)dien-17-one 17-ethylene ketal is a synthetic chemical compound that belongs to the group of estrogen hormones. It is a derivative of estradiol with a methoxy and ethylene ketal group attached to the C17 position of the steroid nucleus. 3-Methoxy-18-methylestra-2,5(10)dien-17-one 17-ethylene ketal possesses unique structural features that make it a promising candidate for medicinal and pharmaceutical research, particularly in the development of hormone-based therapies and treatments for conditions related to hormone imbalances.

19741-72-1

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19741-72-1 Usage

Uses

Used in Pharmaceutical Research:
3-Methoxy-18-methylestra-2,5(10)dien-17-one 17-ethylene ketal is used as a research compound for the development of hormone-based therapies. Its unique structure and properties make it a valuable tool for studying the effects of estrogen hormones and their potential applications in treating various conditions related to hormone imbalances.
Used in Hormone Replacement Therapy:
In the medical industry, 3-Methoxy-18-methylestra-2,5(10)dien-17-one 17-ethylene ketal is used as a hormone replacement agent for conditions such as menopause, where the natural production of estrogen hormones decreases. Its ability to mimic the effects of endogenous estrogens makes it a potential candidate for hormone replacement therapy, helping to alleviate symptoms associated with hormonal imbalances.
Used in Treatment of Hormone-Related Conditions:
3-Methoxy-18-methylestra-2,5(10)dien-17-one 17-ethylene ketal is used as a therapeutic agent for the treatment of various hormone-related conditions, such as polycystic ovary syndrome (PCOS) and endometriosis. Its estrogenic properties can help regulate hormonal levels and alleviate symptoms associated with these conditions.
Used in Drug Development:
In the pharmaceutical industry, 3-Methoxy-18-methylestra-2,5(10)dien-17-one 17-ethylene ketal is used as a lead compound for the development of new drugs targeting hormone-related disorders. Its unique structure and properties provide a foundation for the design and synthesis of novel therapeutic agents with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 19741-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,4 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19741-72:
(7*1)+(6*9)+(5*7)+(4*4)+(3*1)+(2*7)+(1*2)=131
131 % 10 = 1
So 19741-72-1 is a valid CAS Registry Number.

19741-72-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (8'R,9'S,13'S,14'S)-13'-ethyl-3'-methoxyspiro[1,3-dioxolane-2,17'-4,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene]

1.2 Other means of identification

Product number -
Other names Spiro[17H-cyclopenta[a]phenanthrene-17,2'-[1,3]dioxolane],gona-2,5(10)-dien-17-one deriv.

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19741-72-1 SDS

19741-72-1Relevant academic research and scientific papers

SILICA GEL PROMOTED SELECTIVE HYDROLYSIS OF 3-METHOXY-2,5(10)-DIENE STEROIDS

Lui, Li-Gong,Zhang, Tong,Li, Zhen-Su

, p. 2999 - 3006 (2007/10/03)

Hydrolysis of 3-methoxy-2,5(10)-diene steroids (1a-c) via oxalic acid in the presence of silica gel was developed as a fast selective synthesis method toward corresponding 5(10)-en-3-ones (2a-c) in good yield (51-94percent).This also provided a new method for selective ketalisation of 17-keto over 3-keto (2c).

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