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443639-01-8

8-quinolinyl 1-naphthoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 443639-01-8 Structure

  • Basic information

    1. Product Name: 8-quinolinyl 1-naphthoate
    2. Synonyms: 8-quinolinyl 1-naphthoate;quinolin-8-yl naphthalene-1-carboxylate
    3. CAS NO:443639-01-8
    4. Molecular Formula: C20H13NO2
    5. Molecular Weight: 299.32272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 443639-01-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 8-quinolinyl 1-naphthoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-quinolinyl 1-naphthoate(443639-01-8)
    11. EPA Substance Registry System: 8-quinolinyl 1-naphthoate(443639-01-8)

  • 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: 443639-01-8(Hazardous Substances Data)

443639-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 443639-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,6,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 443639-01:
(8*4)+(7*4)+(6*3)+(5*6)+(4*3)+(3*9)+(2*0)+(1*1)=148
148 % 10 = 8
So 443639-01-8 is a valid CAS Registry Number.

443639-01-8Downstream Products

443639-01-8Relevant articles and documents

Quinolin-8-yl Formate: A New Option for Small-Scale Carbonylation Reactions in Microwave Reactors

Maddocks, Christopher J.,Aathimanikandan, Sivakumar V.,Richardson, Jeffery,Ruble, J. Craig

, p. 1608 - 1612 (2020)

A convenient procedure for conducting small-scale carbonylations of aryl or benzyl halides in a microwave reactor by using quinolin-8-yl formate is described. The resulting 8-acyloxyquinolines were shown to be more reactive than phenyl esters in acyl-tran

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