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147218-12-0

4-tert-butoxy-2-(2-fluorophenyl)-7-(trifluoromethyl)quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147218-12-0 Structure

  • Basic information

    1. Product Name: 4-tert-butoxy-2-(2-fluorophenyl)-7-(trifluoromethyl)quinoline
    2. Synonyms:
    3. CAS NO:147218-12-0
    4. Molecular Formula:
    5. Molecular Weight: 363.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147218-12-0.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-butoxy-2-(2-fluorophenyl)-7-(trifluoromethyl)quinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-tert-butoxy-2-(2-fluorophenyl)-7-(trifluoromethyl)quinoline(147218-12-0)
    11. EPA Substance Registry System: 4-tert-butoxy-2-(2-fluorophenyl)-7-(trifluoromethyl)quinoline(147218-12-0)

  • 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: 147218-12-0(Hazardous Substances Data)

147218-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147218-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,1 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 147218-12:
(8*1)+(7*4)+(6*7)+(5*2)+(4*1)+(3*8)+(2*1)+(1*2)=120
120 % 10 = 0
So 147218-12-0 is a valid CAS Registry Number.

147218-12-0Downstream Products

147218-12-0Relevant articles and documents

Synthesis of Fluoro and Trifluoromethyl Derivatives of 2-Phenylquinolin-4-ol

Janda, Lubomir,Nguyen, Johnny,Patterson, Steven E.,Strekowski, Lucjan

, p. 1753 - 1756 (2007/10/02)

A tert-butoxide base-mediated cyclization of fluoro- and trifluoromethyl-substituted Schiff bases 12-19 produces 4-tert-butoxyquinolines 23-30 which are hydrolyzed to quinolin-4-ols 31-38.

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