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293313-21-0

1H-Imidazole, 4,5-bis(4-methylphenyl)-2-(2-thienyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 293313-21-0 Structure

  • Basic information

    1. Product Name: 1H-Imidazole, 4,5-bis(4-methylphenyl)-2-(2-thienyl)-
    2. Synonyms:
    3. CAS NO:293313-21-0
    4. Molecular Formula: C21H18N2S
    5. Molecular Weight: 330.453
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 293313-21-0.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: 1H-Imidazole, 4,5-bis(4-methylphenyl)-2-(2-thienyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Imidazole, 4,5-bis(4-methylphenyl)-2-(2-thienyl)-(293313-21-0)
    11. EPA Substance Registry System: 1H-Imidazole, 4,5-bis(4-methylphenyl)-2-(2-thienyl)-(293313-21-0)

  • 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: 293313-21-0(Hazardous Substances Data)

293313-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 293313-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,3,1 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 293313-21:
(8*2)+(7*9)+(6*3)+(5*3)+(4*1)+(3*3)+(2*2)+(1*1)=130
130 % 10 = 0
So 293313-21-0 is a valid CAS Registry Number.

293313-21-0Relevant articles and documents

Microwave-assisted synthesis of substituted imidazoles on a solid support under solvent-free conditions

Usyatinsky, Alexander Ya.,Khmelnitsky, Yuri L.

, p. 5031 - 5034 (2000)

The solvent-free microwave-assisted synthesis of 2,4,5-substituted and 1,2,4,5-substituted imidazoles is reported. Imidazoles are obtained as a result of the condensation of a 1,2-dicarbonyl compound with an aldehyde and an amine using acidic alumina impregnated with ammonium acetate as the solid support. (C) 2000 Elsevier Science Ltd.

New class of imidazoles incorporated with thiophenevinyl conjugation pathway for robust nonlinear optical chromophores

Santos, Javier,Mintz, Eric A.,Zehnder, Oliver,Bosshard, Christian,Bu, Xiu R.,Günter, Peter

, p. 805 - 808 (2007/10/03)

A new series of thermally stable heterocyclic imidazole-based nonlinear optical chromophores has been developed. These chromophores possess a thiophene based stilbene conjugation pathway with a nitro acceptor group attached to the phenyl end. This feature leads to robust chromopores with high thermal stability and enhanced molecular nonlinearity.

A novel approach to synthesis of tricyanovinylthiophene for heterocyclic imidazole nonlinear optical chromophores

Bu, Xiu R.,Li, Haiying,Van Derveer, Donald,Mintz, Eric A.

, p. 7331 - 7334 (2007/10/03)

A new synthetic method for tricyanovinylation has been developed to prepare a series of novel NLO imidazole chromophores containing a tricyanovinyl acceptor coupled with thiophene spacer.

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