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3-Methoxyestra-1,3,5(10)-trien-16-ol, also known as 3-methoxyestradiol or 3-MeO-E2, is a naturally occurring metabolite of the hormone estradiol, which is the primary female sex hormone. It is a phenolic compound with a molecular formula of C19H24O3 and a molecular weight of 300.39 g/mol. This chemical is characterized by the presence of a methoxy group (-OCH3) at the 3-position of the estratriene backbone and a hydroxyl group (-OH) at the 16-position. 3-Methoxyestradiol plays a role in various physiological processes, including the regulation of the menstrual cycle, bone health, and cardiovascular function. It has also been studied for its potential anti-proliferative effects on certain types of cancer cells.

74111-56-1

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74111-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74111-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,1 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74111-56:
(7*7)+(6*4)+(5*1)+(4*1)+(3*1)+(2*5)+(1*6)=101
101 % 10 = 1
So 74111-56-1 is a valid CAS Registry Number.

74111-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-16-ol

1.2 Other means of identification

Product number -
Other names Mytatrienediol

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:74111-56-1 SDS

74111-56-1Downstream Products

74111-56-1Relevant academic research and scientific papers

Mass spectrometry of ring D hydroxylated 3-methoxy-1,3,5(10)-estratrienes

Schade,Ihn,Vokoun,Schoenecker,Schubert

, p. 547 - 561 (2007/10/02)

Mass spectra and fragmentation patterns of the epimeric 17-,16-,15- and 14-hydroxy derivatives of 3-methoxy- 1,3,5(10)-estratriene are compared. The main fragmentation pathways are differently influenced, depending on the position of the hydroxy group. The different configuration of the hydroxy groups is reflected only in the spectra of the epimeric 15- and 14-hydroxy compounds. Possibilities of mass spectrometric differentiation between the hydroxy-estratrienes are discussed.

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