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144654-11-5

2-methyl(4-N,N-dimethylaminophenyl)amino-4,6-difluoro-s-triazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144654-11-5 Structure

  • Basic information

    1. Product Name: 2-methyl(4-N,N-dimethylaminophenyl)amino-4,6-difluoro-s-triazine
    2. Synonyms:
    3. CAS NO:144654-11-5
    4. Molecular Formula:
    5. Molecular Weight: 265.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144654-11-5.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-methyl(4-N,N-dimethylaminophenyl)amino-4,6-difluoro-s-triazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl(4-N,N-dimethylaminophenyl)amino-4,6-difluoro-s-triazine(144654-11-5)
    11. EPA Substance Registry System: 2-methyl(4-N,N-dimethylaminophenyl)amino-4,6-difluoro-s-triazine(144654-11-5)

  • 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: 144654-11-5(Hazardous Substances Data)

144654-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144654-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,5 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 144654-11:
(8*1)+(7*4)+(6*4)+(5*6)+(4*5)+(3*4)+(2*1)+(1*1)=125
125 % 10 = 5
So 144654-11-5 is a valid CAS Registry Number.

144654-11-5Downstream Products

144654-11-5Relevant articles and documents

Polyhalogenoheterocyclic compounds. Part 40. Tertiary aromatic amines as carbon-nucleophiles with activated perfluorinated aromatic compounds

Chambers,Korn,Sandford

, p. 7939 - 7950 (2007/10/02)

The first examples illustrating that aromatic amines may act as carbon nucleophiles, in reactions with fluorinated aromatic compounds, are described. Products with potential for considerable charge separation are described.

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