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4-tert-Butyl-1-benzyl-1,4-dihydronicotinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147397-80-6 Structure
  • Basic information

    1. Product Name: 4-tert-Butyl-1-benzyl-1,4-dihydronicotinamide
    2. Synonyms: 4-tert-Butyl-1-benzyl-1,4-dihydronicotinamide
    3. CAS NO:147397-80-6
    4. Molecular Formula:
    5. Molecular Weight: 270.374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147397-80-6.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: 4-tert-Butyl-1-benzyl-1,4-dihydronicotinamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-tert-Butyl-1-benzyl-1,4-dihydronicotinamide(147397-80-6)
    11. EPA Substance Registry System: 4-tert-Butyl-1-benzyl-1,4-dihydronicotinamide(147397-80-6)
  • 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: 147397-80-6(Hazardous Substances Data)

147397-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147397-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,3,9 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147397-80:
(8*1)+(7*4)+(6*7)+(5*3)+(4*9)+(3*7)+(2*8)+(1*0)=166
166 % 10 = 6
So 147397-80-6 is a valid CAS Registry Number.

147397-80-6Relevant articles and documents

SIMPLE PREPARATIONS OF C-4-TERT-BUTYLATED NADH/NAD+ ANALOGS

Anne, Agnes

, p. 2331 - 2337 (1992)

The addition of tert-butyl Grignard reagent to the 1-benzyl-3-carbamoylpyridinium salt (1) gives a mixture C-4-(2), C-6-(3), and C-2-tert-butylated dihydronicotinamides (4) in which the desired 1,4-isomer predominates.Stable cristalline 1-benzyl-4-tert-butyl-1,4-dihydronicotinamide (2) can be easily isolated.Oxidation of the product with the 1-benzyl-3-cyanoquinolinium ion (6) was found to be strongly solvent-dependent.In acetonitrile, exclusive hydride transfer gives the corresponding C-4-tert-butylated pyridinium ion (5).In methanol, an interesting tert-butyl transfer from 1,4-dihydronicotinamide (2) to quinolinium (6) occurs competitively, and predominates in the presence of a catalytic amount of formic acid; the resulting C-4-tert-butylated 1,4-dihydroquinoline derivative (8) can be readily isolated.

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