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CAS

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534572-73-1

(15alpha,17beta)-3,17-Dihydroxyestra-1,3,5(10)-triene-15-carboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 534572-73-1 Structure

  • Basic information

    1. Product Name: (15alpha,17beta)-3,17-Dihydroxyestra-1,3,5(10)-triene-15-carboxylic acid ethyl ester
    2. Synonyms:
    3. CAS NO:534572-73-1
    4. Molecular Formula: C21H28O4
    5. Molecular Weight: 344.45491
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 534572-73-1.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: (15alpha,17beta)-3,17-Dihydroxyestra-1,3,5(10)-triene-15-carboxylic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (15alpha,17beta)-3,17-Dihydroxyestra-1,3,5(10)-triene-15-carboxylic acid ethyl ester(534572-73-1)
    11. EPA Substance Registry System: (15alpha,17beta)-3,17-Dihydroxyestra-1,3,5(10)-triene-15-carboxylic acid ethyl ester(534572-73-1)

  • 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: 534572-73-1(Hazardous Substances Data)

534572-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 534572-73-1 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, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 534572-73:
(8*5)+(7*3)+(6*4)+(5*5)+(4*7)+(3*2)+(2*7)+(1*3)=161
161 % 10 = 1
So 534572-73-1 is a valid CAS Registry Number.

534572-73-1Relevant articles and documents

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

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Page/Page column 2; 7; sheet 2, (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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