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1402849-71-1

N-methyl-2-phenyl-1-naphthamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402849-71-1 Structure

  • Basic information

    1. Product Name: N-methyl-2-phenyl-1-naphthamide
    2. Synonyms: N-methyl-2-phenyl-1-naphthamide
    3. CAS NO:1402849-71-1
    4. Molecular Formula:
    5. Molecular Weight: 261.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402849-71-1.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: N-methyl-2-phenyl-1-naphthamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-2-phenyl-1-naphthamide(1402849-71-1)
    11. EPA Substance Registry System: N-methyl-2-phenyl-1-naphthamide(1402849-71-1)

  • 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: 1402849-71-1(Hazardous Substances Data)

1402849-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402849-71-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,8,4 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1402849-71:
(9*1)+(8*4)+(7*0)+(6*2)+(5*8)+(4*4)+(3*9)+(2*7)+(1*1)=151
151 % 10 = 1
So 1402849-71-1 is a valid CAS Registry Number.

1402849-71-1Downstream Products

1402849-71-1Relevant articles and documents

Regioselective ortho-arylation and alkenylation of N-alkyl benzamides with boronic acids via ruthenium-catalyzed C-H bond activation: An easy route to fluorenones synthesis

Chinnagolla, Ravi Kiran,Jeganmohan, Masilamani

, p. 5246 - 5249,4 (2012)

A highly regioselective ruthenium-catalyzed ortho-arylation of substituted N-alkyl benzamides with aromatic boronic acids in the presence of [{RuCl 2(p-cymene)}2], AgSbF6, and Ag2O is described. Further, ortho-arylated N-alkyl benzamides were converted into fluorenones in the presence of trifluoroacetic anhydride and HCl.

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