17976-32-8 Usage
Description
2,5(10)-ESTRADIEN-3-OL-17-ONE 3-METHYL ETHER, also known as 3-Methoxyestra-2,5(10)-dien-17-one, is a chemical compound that is structurally related to 3-O-Methyl Estrone (M304710). It is an estrogenic hormone, which means it has the ability to mimic the effects of estrogen in the body.
Uses
Used in Pharmaceutical Industry:
2,5(10)-ESTRADIEN-3-OL-17-ONE 3-METHYL ETHER is used as a pharmaceutical agent for its estrogenic properties. It can be used in the development of hormone replacement therapies or treatments for conditions related to hormonal imbalances.
Used in Research Applications:
2,5(10)-ESTRADIEN-3-OL-17-ONE 3-METHYL ETHER is used as a research compound for studying the effects of estrogen on various biological processes. It can be used to investigate the role of estrogen in reproductive health, bone health, and other physiological functions.
Used in Cosmetic Industry:
2,5(10)-ESTRADIEN-3-OL-17-ONE 3-METHYL ETHER can be used as an ingredient in cosmetic products for its potential anti-aging and skin health benefits. Its estrogenic properties may help improve skin elasticity, reduce wrinkles, and promote a more youthful appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 17976-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,7 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17976-32:
(7*1)+(6*7)+(5*9)+(4*7)+(3*6)+(2*3)+(1*2)=148
148 % 10 = 8
So 17976-32-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H26O2/c1-19-10-9-15-14-6-4-13(21-2)11-12(14)3-5-16(15)17(19)7-8-18(19)20/h4,15-17H,3,5-11H2,1-2H3
17976-32-8Relevant articles and documents
METHOD FOR SYNTHESIS OF DIENOGEST FROM ESTRONE-3-METHYLETHER
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Page/Page column 3, (2010/12/29)
A method for the synthesis of dienogest from 3-methoxy-estra-1,3,5-trien-17-one includes the steps of a) reacting 3-methoxy-estra-1,3,5-trien-17-one with alcohol in the presence of an acid in an organic solvent to form 3-methoxy-17,17-dialkoxy-estra-1,3,5
Total-synthesis of (-)-norgestrel
Baier,Durner,Quinkert
, p. 1054 - 1068 (2007/10/02)
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Synthesis of 13-alkyl-gon-4-ones
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, (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.
