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663192-17-4

Butanamide, N-(2-bromophenyl)-4,4,4-trifluoro-3-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 663192-17-4 Structure

  • Basic information

    1. Product Name: Butanamide, N-(2-bromophenyl)-4,4,4-trifluoro-3-oxo-
    2. Synonyms:
    3. CAS NO:663192-17-4
    4. Molecular Formula: C10H7BrF3NO2
    5. Molecular Weight: 310.07
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 663192-17-4.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: Butanamide, N-(2-bromophenyl)-4,4,4-trifluoro-3-oxo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanamide, N-(2-bromophenyl)-4,4,4-trifluoro-3-oxo-(663192-17-4)
    11. EPA Substance Registry System: Butanamide, N-(2-bromophenyl)-4,4,4-trifluoro-3-oxo-(663192-17-4)

  • 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: 663192-17-4(Hazardous Substances Data)

663192-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 663192-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,3,1,9 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 663192-17:
(8*6)+(7*6)+(6*3)+(5*1)+(4*9)+(3*2)+(2*1)+(1*7)=164
164 % 10 = 4
So 663192-17-4 is a valid CAS Registry Number.

663192-17-4Downstream Products

663192-17-4Relevant articles and documents

An Improved Access to 4-Trifluoromethyl-2(1H)-quinolinones: The "Watering Protocol"

Marull, Marc,Lefebvre, Olivier,Schlosser, Manfred

, p. 54 - 63 (2004)

Condensation of anilines with ethyl 4,4,4-trifluoroacetoacetate (7) to afford the corresponding 4,4,4-trifluoro-3-oxobutaneanilides (10), precursors to 4-(trifluoromethyl)-2-quinolinones (11), can be favored and the competing condensation to produce the e

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