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101978-01-2

3-Methoxy-estra-2,5(10)-dien-17-ol, also known as 3-Methoxy-estra-2,5(10)-dien-17β-ol, is a synthetic estrogenic compound belonging to the estra-2,5(10)-dienes class. Derived from estradiol, it features a methoxy group at the 3 position on the steroid ring, exhibiting notable estrogenic properties. Primarily utilized as a research chemical, it is not approved for human consumption and requires further research to elucidate its pharmacological properties and potential applications, particularly in hormone therapy and its impact on reproductive health and development.

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  • 101978-01-2 Structure

  • Basic information

    1. Product Name: 3-Methoxy-estra-2,5(10)-dien-17-ol
    2. Synonyms: 3-Methoxy-estra-2,5(10)-dien-17-ol;Birch-Me;3-methyl-1-[2-[2-(3-methylquinuclidin-1-ium-1-yl)ethoxy]ethyl]quinuclidin-1-ium;8-methyl-1-[2-[2-(8-methyl-1-azoniabicyclo[2.2.2]octan-1-yl)ethoxy]ethyl]-1-azoniabicyclo[2.2.2]octane
    3. CAS NO:101978-01-2
    4. Molecular Formula: C19H28O2
    5. Molecular Weight: 288.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101978-01-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 437.1±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.11±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 15.04±0.60(Predicted)
    10. CAS DataBase Reference: 3-Methoxy-estra-2,5(10)-dien-17-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Methoxy-estra-2,5(10)-dien-17-ol(101978-01-2)
    12. EPA Substance Registry System: 3-Methoxy-estra-2,5(10)-dien-17-ol(101978-01-2)

  • 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: 101978-01-2(Hazardous Substances Data)

101978-01-2 Usage

Uses

Used in Pharmaceutical Research:
3-Methoxy-estra-2,5(10)-dien-17-ol is used as a research chemical for studying its estrogenic properties and potential applications in hormone therapy. It aids in understanding the compound's effects on reproductive health and development, contributing to the advancement of pharmaceutical knowledge in the field of endocrinology.
Used in Hormone Therapy Research:
In the field of hormone therapy, 3-Methoxy-estra-2,5(10)-dien-17-ol is used as a research compound to explore its potential role in treating conditions related to hormonal imbalances. Its estrogenic properties make it a candidate for further investigation into its therapeutic effects and safety profile.

Check Digit Verification of cas no

The CAS Registry Mumber 101978-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,7 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 101978-01:
(8*1)+(7*0)+(6*1)+(5*9)+(4*7)+(3*8)+(2*0)+(1*1)=112
112 % 10 = 2
So 101978-01-2 is a valid CAS Registry Number.

101978-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxy-estra-2,5(10)-dien-17-ol

1.2 Other means of identification

Product number -
Other names 8-methyl-1-[2-[2-(8-methyl-1-azoniabicyclo[2.2.2]octan-1-yl)ethoxy]ethyl]-1-azoniabicyclo[2.2.2]octane

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:101978-01-2 SDS

101978-01-2Relevant articles and documents

Synthesis of ent-17-(prop-1-ynyl-17β-hydroxy-11β-(4-(N,N-dimethylamino)-phenyl)-4,9- estradien-3-one, the antipode of RU - 38 486

Ottow,Beier,Elger,Henderson,Neef,Wiechert

, p. 519 - 530 (2007/10/02)

The title compound was synthesized and tested for its biological activities. It showed neither antiprogesterone nor antiglucocorticoid properties.

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