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CAS

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132363-86-1

1-methyl-2-(trichloromethyl)-1,2-dihydroquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132363-86-1 Structure

  • Basic information

    1. Product Name: 1-methyl-2-(trichloromethyl)-1,2-dihydroquinoline
    2. Synonyms: 1-methyl-2-(trichloromethyl)-1,2-dihydroquinoline
    3. CAS NO:132363-86-1
    4. Molecular Formula: C11H10Cl3N
    5. Molecular Weight: 262.5628
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132363-86-1.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: 1-methyl-2-(trichloromethyl)-1,2-dihydroquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methyl-2-(trichloromethyl)-1,2-dihydroquinoline(132363-86-1)
    11. EPA Substance Registry System: 1-methyl-2-(trichloromethyl)-1,2-dihydroquinoline(132363-86-1)

  • 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: 132363-86-1(Hazardous Substances Data)

132363-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132363-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132363-86:
(8*1)+(7*3)+(6*2)+(5*3)+(4*6)+(3*3)+(2*8)+(1*6)=111
111 % 10 = 1
So 132363-86-1 is a valid CAS Registry Number.

132363-86-1Relevant articles and documents

Convenient synthesis of trichloromethyldihydroquinolines and -isoquinolines

Grignon-Dubois,Diaba,Grellier-Marly

, p. 800 - 804 (1994)

The reaction of a series of N-alkylquinolinium and -isoquinolinium iodides towards sodium trichloroacetate in acetonitrile has been investigated under reflux or ultrasonication. In all cases, addition of trichloromethyl anion was observed, and trichloromethyldihydroquinoline or -isoquinoline derivatives were obtained in good yields. Depending on the activation process, addition occurred at the 2- or the 4-position with quinolines and at the 1-position with isoquinolines.

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