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CAS

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153004-08-1

3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol is an estradiol derivative, which is a modified form of the naturally occurring hormone estradiol. 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol features a 3-methoxy group and a 6-phenylsulfonyl group, and it is characterized by its light brown solid appearance. It is primarily used in the chemical synthesis of alkylated estratrienes, which are important in various pharmaceutical applications.

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  • 153004-08-1 Structure

  • Basic information

    1. Product Name: 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol
    2. Synonyms: 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol;(17β)-3-Methoxy-6-(phenylsulfonyl)-estra-1,3,5(10),6-tetraen-17-ol Acetate
    3. CAS NO:153004-08-1
    4. Molecular Formula: C27H30O5S
    5. Molecular Weight: 466.5891
    6. EINECS: N/A
    7. Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids
    8. Mol File: 153004-08-1.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: Dichloromethane
    9. CAS DataBase Reference: 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol(153004-08-1)
    11. EPA Substance Registry System: 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol(153004-08-1)

  • 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: 153004-08-1(Hazardous Substances Data)

153004-08-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol is used as an intermediate in the preparation of alkylated estratrienes for the pharmaceutical industry. These alkylated estratrienes are significant in the development of medications targeting hormone-related conditions and diseases.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol serves as a key compound in the synthesis of various estratriene-based molecules. Its unique structural features make it a valuable building block for creating new pharmaceutical agents with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 153004-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,0 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 153004-08:
(8*1)+(7*5)+(6*3)+(5*0)+(4*0)+(3*4)+(2*0)+(1*8)=81
81 % 10 = 1
So 153004-08-1 is a valid CAS Registry Number.

153004-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [(8R,9S,13S,14S,17R)-6-(benzenesulfonyl)-3-methoxy-13-methyl-8,9,11,12,14,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl] acetate

1.2 Other means of identification

Product number -
Other names 3-Methoxy-6-phenylsulfonyl-6,7-didehydro Estradiol

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:153004-08-1 SDS

153004-08-1Downstream Products

153004-08-1Relevant articles and documents

A NEW, STEREOSELECTIVE APPROACH TO C(7)-ALKYLATED ESTRA-1,3,5(10)-TRIENE DERIVATIVES

Kuenzer, H.,Thiel, M.,Sauer, G.,Wiechert, R.

, p. 1691 - 1694 (2007/10/02)

17β-Acetyloxy-3-methoxy-6-(phenylsulfonyl)estra-1,3,5(10),6-tetraene (4) was prepared as a substrate for conjugate addition of organolithium reagents by a three-step sequence starting from 17β-acetyloxy-3-methoxyestra-1,3,5(10)-trien-6-one (2).While methy

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