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CAS

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65754-01-0

17β-acetoxy-estratriene-(5.7.9) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65754-01-0 Structure

  • Basic information

    1. Product Name: 17β-acetoxy-estratriene-(5.7.9)
    2. Synonyms:
    3. CAS NO:65754-01-0
    4. Molecular Formula:
    5. Molecular Weight: 298.425
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65754-01-0.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-acetoxy-estratriene-(5.7.9)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 17β-acetoxy-estratriene-(5.7.9)(65754-01-0)
    11. EPA Substance Registry System: 17β-acetoxy-estratriene-(5.7.9)(65754-01-0)

  • 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: 65754-01-0(Hazardous Substances Data)

65754-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65754-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,5 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65754-01:
(7*6)+(6*5)+(5*7)+(4*5)+(3*4)+(2*0)+(1*1)=140
140 % 10 = 0
So 65754-01-0 is a valid CAS Registry Number.

65754-01-0Downstream Products

65754-01-0Relevant articles and documents

Catalytic hydrogenation on Raney nickel of estra-1,3,5(10),8,14-pentaenes with sterically accessible double bonds

Morozkina,Nikolaev,Selivanov,Ushakov,Shavva

, p. 675 - 680 (2008)

The catalytic hydrogenation of estra-1,3,5(10),8,14-pentaenes with sterically accessible double bonds in the presence of Raney nickel in 2-propanol at elevated pressure and at heating to 110-120°C resulted in prevailing formation of estrogens 8α-analogs alongside a considerable quantity of estra-5,7,9-trienes. Although the hydrogenation at 45-60°C provided a higher yield of estrogens 8α-analogs, the synthesis of steroids of this group gave better results at hydrogenation in a high purity benzene.

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