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CAS

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1190130-53-0

4-(4-chlorobenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1190130-53-0 Structure

  • Basic information

    1. Product Name: 4-(4-chlorobenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine
    2. Synonyms:
    3. CAS NO:1190130-53-0
    4. Molecular Formula:
    5. Molecular Weight: 315.726
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1190130-53-0.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-(4-chlorobenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-chlorobenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(1190130-53-0)
    11. EPA Substance Registry System: 4-(4-chlorobenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(1190130-53-0)

  • 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: 1190130-53-0(Hazardous Substances Data)

1190130-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1190130-53-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,1,3 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1190130-53:
(9*1)+(8*1)+(7*9)+(6*0)+(5*1)+(4*3)+(3*0)+(2*5)+(1*3)=110
110 % 10 = 0
So 1190130-53-0 is a valid CAS Registry Number.

1190130-53-0Downstream Products

1190130-53-0Relevant articles and documents

α-Trifluoromethyl-β-aryl enamines in the synthesis of trifluoromethylated heterocycles by the Fischer and the Pictet-Spengler reactions

Muzalevskiy, Vasiliy M.,Nenajdenko, Valentine G.,Shastin, Aleksey V.,Balenkova, Elizabeth S.,Haufe, Günter

experimental part, p. 7553 - 7561 (2009/12/06)

α-Trifluoromethyl-β-aryl enamines were successfully used as synthetic equivalents of benzyltrifluoromethyl ketones in both the Fischer indole synthesis and the Pictet-Spengler reaction. Accordingly, 2-trifluoromethyl indoles and a variety of trifluorometh

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