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CAS

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160849-90-1

2,5-Ditrifluoromethanesulfonyloxybenzophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160849-90-1 Structure

  • Basic information

    1. Product Name: 2,5-Ditrifluoromethanesulfonyloxybenzophenone
    2. Synonyms: 2,5-Ditrifluoromethanesulfonyloxybenzophenone
    3. CAS NO:160849-90-1
    4. Molecular Formula:
    5. Molecular Weight: 478.347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160849-90-1.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: 2,5-Ditrifluoromethanesulfonyloxybenzophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-Ditrifluoromethanesulfonyloxybenzophenone(160849-90-1)
    11. EPA Substance Registry System: 2,5-Ditrifluoromethanesulfonyloxybenzophenone(160849-90-1)

  • 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: 160849-90-1(Hazardous Substances Data)

160849-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160849-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,8,4 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 160849-90:
(8*1)+(7*6)+(6*0)+(5*8)+(4*4)+(3*9)+(2*9)+(1*0)=151
151 % 10 = 1
So 160849-90-1 is a valid CAS Registry Number.

160849-90-1Relevant articles and documents

Synthesis of benzodiazepines

-

, (2008/06/13)

A general method is provided for the synthesis of substituted 2,3-dihydro-5-phenyl-1H-1,4-benzodiazepines by the reaction of bis-trifiated-2,5-dihydroxy benzophenones with 1,2-bisaminoethanes, followed by displacement of the 7-trifloxy group.

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