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1258870-74-4

4,5-dichloro-1,3-bis(4-cyanobenzyl)imidazolium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1258870-74-4 Structure

  • Basic information

    1. Product Name: 4,5-dichloro-1,3-bis(4-cyanobenzyl)imidazolium bromide
    2. Synonyms:
    3. CAS NO:1258870-74-4
    4. Molecular Formula:
    5. Molecular Weight: 448.149
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1258870-74-4.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: 4,5-dichloro-1,3-bis(4-cyanobenzyl)imidazolium bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,5-dichloro-1,3-bis(4-cyanobenzyl)imidazolium bromide(1258870-74-4)
    11. EPA Substance Registry System: 4,5-dichloro-1,3-bis(4-cyanobenzyl)imidazolium bromide(1258870-74-4)

  • 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: 1258870-74-4(Hazardous Substances Data)

1258870-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258870-74-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,8,7 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1258870-74:
(9*1)+(8*2)+(7*5)+(6*8)+(5*8)+(4*7)+(3*0)+(2*7)+(1*4)=194
194 % 10 = 4
So 1258870-74-4 is a valid CAS Registry Number.

1258870-74-4Downstream Products

1258870-74-4Relevant articles and documents

Synthesis, cytotoxicity and antibacterial studies of symmetrically and non-symmetrically benzyl- or p-cyanobenzyl-substituted N-Heterocyclic carbene - Silver complexes

Patil, Siddappa,Deally, Anthony,Gleeson, Brendan,Mueller-Bunz, Helge,Paradisi, Francesca,Tacke, Matthias

, p. 781 - 793 (2010)

From the reaction of 1H-imidazole (1a), 4,5-dichloro-1H-imidazole (1b) and 1H-benzimidazole (1c) with p-cyanobenzyl bromide (2), symmetrically substituted N-heterocyclic carbene (NHC) [(3a-c)] precursors, 1-methylimidazole (5a), 4,5-dichloro-1-methylimida

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