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1507365-51-6

C17H16Cl2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1507365-51-6 Structure

  • Basic information

    1. Product Name: C17H16Cl2O2
    2. Synonyms:
    3. CAS NO:1507365-51-6
    4. Molecular Formula:
    5. Molecular Weight: 323.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1507365-51-6.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: C17H16Cl2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H16Cl2O2(1507365-51-6)
    11. EPA Substance Registry System: C17H16Cl2O2(1507365-51-6)

  • 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: 1507365-51-6(Hazardous Substances Data)

1507365-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1507365-51-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,0,7,3,6 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1507365-51:
(9*1)+(8*5)+(7*0)+(6*7)+(5*3)+(4*6)+(3*5)+(2*5)+(1*1)=156
156 % 10 = 6
So 1507365-51-6 is a valid CAS Registry Number.

1507365-51-6Relevant articles and documents

Enantioselective oxidation of 1,2-diols with quinine-derived urea organocatalyst

Rong, Zi-Qiang,Pan, Hui-Jie,Yan, Hai-Long,Zhao, Yu

supporting information, p. 208 - 211 (2014/01/23)

Quinine-derived urea has been identified as a highly efficient organocatalyst for the enantioselective oxidation of 1,2-diols using bromination reagents as the oxidant. This simple procedure utilizes readily available reagents and operates at ambient temperature to yield a wide range of α-hydroxy ketones in good yield (up to 94%) and excellent enantioselectivity (up to 95% ee).

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