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515845-47-3

Quinoline, 2-ethyl-4-(trifluoromethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 515845-47-3 Structure

  • Basic information

    1. Product Name: Quinoline, 2-ethyl-4-(trifluoromethyl)- (9CI)
    2. Synonyms: Quinoline, 2-ethyl-4-(trifluoromethyl)- (9CI)
    3. CAS NO:515845-47-3
    4. Molecular Formula: C12H10F3N
    5. Molecular Weight: 225.2097096
    6. EINECS: N/A
    7. Product Categories: ETHYL
    8. Mol File: 515845-47-3.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: Quinoline, 2-ethyl-4-(trifluoromethyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Quinoline, 2-ethyl-4-(trifluoromethyl)- (9CI)(515845-47-3)
    11. EPA Substance Registry System: Quinoline, 2-ethyl-4-(trifluoromethyl)- (9CI)(515845-47-3)

  • 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: 515845-47-3(Hazardous Substances Data)

515845-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 515845-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,5,8,4 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 515845-47:
(8*5)+(7*1)+(6*5)+(5*8)+(4*4)+(3*5)+(2*4)+(1*7)=163
163 % 10 = 3
So 515845-47-3 is a valid CAS Registry Number.

515845-47-3Downstream Products

515845-47-3Relevant articles and documents

Quinoline formation via a modified Combes reaction: Examination of kinetics, substituent effects, and mechanistic pathways

Sloop, Joseph C.

experimental part, p. 110 - 117 (2010/04/05)

A comprehensive product regioselectlvity and kinetics study of the modified Combes quinoline synthesis shown below has been undertaken: This is the first reported investigation of the Combes condensation employing 19F NMR spectroscopy to monitor intermedi

Synthesis of fluorinated heterocycles

Sloop, Joseph C.,Bumgardner, Carl L.,Loehle, W. David

, p. 135 - 147 (2007/10/03)

Selected 1,3-diketones having a trifluoromethyl group and/or a fluorine in the 2-position were condensed with aromatic hydrazines, hydroxylamine, urea, thiourea, guanidine, and substituted anilines producing pyrazoles, isoxazoles, pyrimidines, and quinolines, respectively, in yields ranging from 27 to 87%.

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