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13587-68-3

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. Additionally, it has 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.

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  • 13587-68-3 Structure

  • Basic information

    1. Product Name: 3MeE2-8-en
    2. Synonyms: 3MEE2-8-EN;(17b)-3-Methoxyestra-1,3,5(10),8(9)-tetraen-17-ol;(17β)-3-methoxy-Estra-1,3,5(1
    3. CAS NO:13587-68-3
    4. Molecular Formula: C19H24O2
    5. Molecular Weight: 284.39266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13587-68-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3MeE2-8-en(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3MeE2-8-en(13587-68-3)
    11. EPA Substance Registry System: 3MeE2-8-en(13587-68-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 13587-68-3(Hazardous Substances Data)

13587-68-3 Usage

Uses

Used in Hormone Replacement Therapy:
3MeE2-8-en is used as a hormone replacement agent for managing menopausal symptoms. Its estrogenic activity helps alleviate symptoms associated with the hormonal changes that occur during menopause, such as hot flashes, night sweats, and vaginal dryness.
Used in Osteoporosis Treatment:
3MeE2-8-en is used as a treatment for osteoporosis to help increase bone density and reduce the risk of fractures. Its estrogenic properties contribute to the maintenance of bone health by promoting bone formation and reducing bone resorption.
Used in Contraceptive Applications:
3MeE2-8-en is used as a contraceptive agent due to its potential to prevent ovulation and fertilization. Its hormonal effects can help regulate the menstrual cycle and reduce the chances of pregnancy.
Used in Cancer Research:
3MeE2-8-en is used in cancer research for its potential anti-cancer properties. Studies are being conducted to explore its effects on various types of cancer and its potential as a therapeutic agent in cancer treatment.
Used in Pharmaceutical Industry:
3MeE2-8-en is used in the pharmaceutical industry for the development of drugs targeting hormone-related conditions. Its estrogenic activity and potential therapeutic applications make it a valuable compound for research and drug development.

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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