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918331-45-0

17β-methyl-16β-phenyl-17α-(2-fluorophenyl)acetoxy-D-homoandrost-4,6-diene-3,17a-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 918331-45-0 Structure

  • Basic information

    1. Product Name: 17β-methyl-16β-phenyl-17α-(2-fluorophenyl)acetoxy-D-homoandrost-4,6-diene-3,17a-dione
    2. Synonyms:
    3. CAS NO:918331-45-0
    4. Molecular Formula:
    5. Molecular Weight: 540.675
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 918331-45-0.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: 17β-methyl-16β-phenyl-17α-(2-fluorophenyl)acetoxy-D-homoandrost-4,6-diene-3,17a-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 17β-methyl-16β-phenyl-17α-(2-fluorophenyl)acetoxy-D-homoandrost-4,6-diene-3,17a-dione(918331-45-0)
    11. EPA Substance Registry System: 17β-methyl-16β-phenyl-17α-(2-fluorophenyl)acetoxy-D-homoandrost-4,6-diene-3,17a-dione(918331-45-0)

  • 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: 918331-45-0(Hazardous Substances Data)

918331-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918331-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,3,3 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 918331-45:
(8*9)+(7*1)+(6*8)+(5*3)+(4*3)+(3*1)+(2*4)+(1*5)=170
170 % 10 = 0
So 918331-45-0 is a valid CAS Registry Number.

918331-45-0Downstream Products

918331-45-0Relevant articles and documents

New-D-homoandrost-4,6-diene derivatives as potent progesterone receptor antagonist

Cabeza, Marisa,Garcia-Lorenzana, Mario,Garces, Montserrat,Heuze, Ivonne,Teran, Nayeli,Bratoeff, Eugene

, p. 101 - 108 (2010)

The aim of this study was to synthesize three different D-homoandrostadiene derivatives (2-4) and study their biological activity. We carried out in vivo and in vitro experiments using female cycling mice, which were synchronized for estrus with luteinizi

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