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1195791-22-0

C18H20BrN3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1195791-22-0 Structure

  • Basic information

    1. Product Name: C18H20BrN3
    2. Synonyms: C18H20BrN3
    3. CAS NO:1195791-22-0
    4. Molecular Formula:
    5. Molecular Weight: 358.281
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1195791-22-0.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: C18H20BrN3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H20BrN3(1195791-22-0)
    11. EPA Substance Registry System: C18H20BrN3(1195791-22-0)

  • 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: 1195791-22-0(Hazardous Substances Data)

1195791-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1195791-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,5,7,9 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1195791-22:
(9*1)+(8*1)+(7*9)+(6*5)+(5*7)+(4*9)+(3*1)+(2*2)+(1*2)=190
190 % 10 = 0
So 1195791-22-0 is a valid CAS Registry Number.

1195791-22-0Relevant articles and documents

Ligand-free copper-catalyzed synthesis of substituted benzimidazoles, 2-aminobenzimidazoles, 2-aminobenzothiazoles, and benzoxazoles

Saha, Prasenjit,Ramana, Tamminana,Purkait, Nibadita,Ali, Md. Ashif,Paul, Rajesh,Punniyamurthy, Tharmalingam

body text, p. 8719 - 8725 (2010/02/28)

(Chemical Equation Presented) The synthesis of substituted benzimidazoles, 2-aminobenzimidazoles, 2-aminobenzothiazoles, and benzoxazoles is described via intramolecular cyclization of o-bromoaryl derivatives using copper(II) oxide nanoparticles in DMSO under air. The procedure is experimentally simple, general, efficient, and free from addition of external chelating ligands. It is a heterogeneous process and the copper(II) oxide nanoparticles can be recovered and recycled without loss of activity. 2009 American Chemical Society.

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