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CAS

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1428867-06-4

5-methyl-2-(1-phenylethoxy)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428867-06-4 Structure

  • Basic information

    1. Product Name: 5-methyl-2-(1-phenylethoxy)pyridine
    2. Synonyms: 5-methyl-2-(1-phenylethoxy)pyridine
    3. CAS NO:1428867-06-4
    4. Molecular Formula:
    5. Molecular Weight: 213.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428867-06-4.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: 5-methyl-2-(1-phenylethoxy)pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-methyl-2-(1-phenylethoxy)pyridine(1428867-06-4)
    11. EPA Substance Registry System: 5-methyl-2-(1-phenylethoxy)pyridine(1428867-06-4)

  • 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: 1428867-06-4(Hazardous Substances Data)

1428867-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428867-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,8,6 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1428867-06:
(9*1)+(8*4)+(7*2)+(6*8)+(5*8)+(4*6)+(3*7)+(2*0)+(1*6)=194
194 % 10 = 4
So 1428867-06-4 is a valid CAS Registry Number.

1428867-06-4Relevant articles and documents

Ir(I)-catalyzed synthesis of N-substituted pyridones from 2-alkoxypyridines via C-O bond cleavage

Pan, Shiguang,Ryu, Naoto,Shibata, Takanori

, p. 1902 - 1905 (2013)

A cationic Ir(I) complex-catalyzed O-to-N-alkyl migration in 2-alkoxypyridines bearing a secondary alkyl group on the oxygen atom by C-O bond cleavage is described. The present transformation gave various N-alkylpyridones in moderate to good yields. The addition of sodium acetate played a key role in suppressing β-hydrogen elimination.

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