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1358531-78-8

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  • 1358531-78-8 Structure

  • Basic information

    1. Product Name: 1-benzyl-3-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)quinolin-4(1H)-one
    2. Synonyms: 1-benzyl-3-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)quinolin-4(1H)-one
    3. CAS NO:1358531-78-8
    4. Molecular Formula:
    5. Molecular Weight: 451.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1358531-78-8.mol
    9. Article Data: 1

  • 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: 1-benzyl-3-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)quinolin-4(1H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-3-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)quinolin-4(1H)-one(1358531-78-8)
    11. EPA Substance Registry System: 1-benzyl-3-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)quinolin-4(1H)-one(1358531-78-8)

  • 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: 1358531-78-8(Hazardous Substances Data)

1358531-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1358531-78-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,8,5,3 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1358531-78:
(9*1)+(8*3)+(7*5)+(6*8)+(5*5)+(4*3)+(3*1)+(2*7)+(1*8)=178
178 % 10 = 8
So 1358531-78-8 is a valid CAS Registry Number.

1358531-78-8Downstream Products

1358531-78-8Relevant articles and documents

Pd-catalyzed dehydrogenative cross-coupling of polyfluoroarenes with heteroatom-substituted enones

Chen, Fei,Feng, Zhang,He, Chun-Yang,Wang, Hao-Yang,Guo, Yin-Long,Zhang, Xingang

supporting information; experimental part, p. 1176 - 1179 (2012/04/04)

The first example of intermolecular regioselective α-arylation of heteroatom-substituted enones with polyfluoroarenes via twofold C-H bond functionalization using a palladium catalyst is reported. This approach provides rapid access to a wide range of α-fluoroarylated enones of interest in life science.

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