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13587-68-3

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13587-68-3 Usage

General Description

3MeE2-8-en, also known as 3-methoxy-17-ethynylestra-1,3,5(10)-triene, is a synthetic steroid compound that belongs to the class of estrogens. It is a derivative of estradiol with an ethynyl group at the 17α position and a methoxy group at the 3 position. 3MeE2-8-en has been studied for its potential use in hormone replacement therapy and as a potential treatment for conditions such as menopausal symptoms and osteoporosis. It has also shown potential as a contraceptive agent and has been investigated for its anti-cancer properties. 3MeE2-8-en has demonstrated estrogenic activity and has been evaluated for its potential clinical applications in various research studies.

Check Digit Verification of cas no

The CAS Registry Mumber 13587-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,8 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13587-68:
(7*1)+(6*3)+(5*5)+(4*8)+(3*7)+(2*6)+(1*8)=123
123 % 10 = 3
So 13587-68-3 is a valid CAS Registry Number.

13587-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3MeE2-8-en

1.2 Other means of identification

Product number -
Other names -

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:13587-68-3 SDS

13587-68-3Relevant articles and documents

Stereocontrolled derivatization of 3-methoxyestra-1,3,5(10), n-tetraenes via lewis acid promoted prins reactions, (n=7; 8(9))

Kuenzer, Hermann,Sauer, Gerhard,Wiechert, Rudolf

, p. 743 - 746 (2007/10/02)

Steroidal olefins 1 and 3 undergo dimethylaluminum chloride-mediated Prins reactions with paraformaldehyde to furnish homoallylic alcohols 4 and 16 as major products. These ene reaction-type intermediates are converted into 6 and 17 by hydroxyl group-assi

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