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534572-93-5

15α-allyl-3-benzyloxyestra-1,3,5(10)-trien-17β-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 534572-93-5 Structure

  • Basic information

    1. Product Name: 15α-allyl-3-benzyloxyestra-1,3,5(10)-trien-17β-ol
    2. Synonyms: 15α-allyl-3-benzyloxyestra-1,3,5(10)-trien-17β-ol
    3. CAS NO:534572-93-5
    4. Molecular Formula:
    5. Molecular Weight: 402.577
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 534572-93-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 15α-allyl-3-benzyloxyestra-1,3,5(10)-trien-17β-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 15α-allyl-3-benzyloxyestra-1,3,5(10)-trien-17β-ol(534572-93-5)
    11. EPA Substance Registry System: 15α-allyl-3-benzyloxyestra-1,3,5(10)-trien-17β-ol(534572-93-5)

  • 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: 534572-93-5(Hazardous Substances Data)

534572-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 534572-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,4,5,7 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 534572-93:
(8*5)+(7*3)+(6*4)+(5*5)+(4*7)+(3*2)+(2*9)+(1*3)=165
165 % 10 = 5
So 534572-93-5 is a valid CAS Registry Number.

534572-93-5Relevant articles and documents

15Alpha-substituted estradiol carboxylic acid esters as locally active estrogens

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Page/Page column 2; 10; sheet 4, (2010/02/08)

The present invention relates to analogs of estradiol, which, in their most preferred embodiment, act as locally active estrogens without significant systemic action. A series of 15α-estradiol ester compounds is presented which exhibit excellent biologica

Synthesis and evaluation of B-, C-, and D-ring-substituted estradiol carboxylic acid esters as locally active estrogens

Labaree, David C.,Zhang, Jing-Xin,Harris, Heather A.,O'Connor, Craig,Reynolds, Toni Y.,Hochberg, Richard B.

, p. 1886 - 1904 (2007/10/03)

We have synthesized derivatives of estradiol that are structurally modified to serve as "soft" estrogens and act within a geographically limited area of the body; estrogens without systemic action. We have previously shown with 16α-substituted analogues o

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