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N-(1H-BENZOIMIDAZOL-2-YL)-BENZENE-1,4-DIAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133929-18-7 Structure
  • Basic information

    1. Product Name: N-(1H-BENZOIMIDAZOL-2-YL)-BENZENE-1,4-DIAMINE
    2. Synonyms: ASINEX-REAG BAS 00547125;4-N-(1H-benzimidazol-2-yl)benzene-1,4-diamine;N-(1H-BENZOIMIDAZOL-2-YL)-BENZENE-1,4-DIAMINE
    3. CAS NO:133929-18-7
    4. Molecular Formula: C13H12N4
    5. Molecular Weight: 224.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133929-18-7.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: N-(1H-BENZOIMIDAZOL-2-YL)-BENZENE-1,4-DIAMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1H-BENZOIMIDAZOL-2-YL)-BENZENE-1,4-DIAMINE(133929-18-7)
    11. EPA Substance Registry System: N-(1H-BENZOIMIDAZOL-2-YL)-BENZENE-1,4-DIAMINE(133929-18-7)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 133929-18-7(Hazardous Substances Data)

133929-18-7 Usage

Uses

N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine can be used to fight emerging viruses.

Check Digit Verification of cas no

The CAS Registry Mumber 133929-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,2 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133929-18:
(8*1)+(7*3)+(6*3)+(5*9)+(4*2)+(3*9)+(2*1)+(1*8)=137
137 % 10 = 7
So 133929-18-7 is a valid CAS Registry Number.

133929-18-7Relevant articles and documents

From Cells to Mice to Target: Characterization of NEU-1053 (SB-443342) and Its Analogues for Treatment of Human African Trypanosomiasis

Devine, William G.,Diaz-Gonzalez, Rosario,Ceballos-Perez, Gloria,Rojas, Domingo,Satoh, Takashi,Tear, Westley,Ranade, Ranae M.,Barros-álvarez, Ximena,Hol, Wim G. J.,Buckner, Frederick S.,Navarro, Miguel,Pollastri, Michael P.

, p. 225 - 236 (2017/04/21)

Human African trypanosomiasis is a neglected tropical disease that is lethal if left untreated. Existing therapeutics have limited efficacy and severe associated toxicities. 2-(2-(((3-((1H-Benzo[d]imidazol-2-yl)amino)propyl)amino)methyl)-4,6-dichloro-1H-indol-1-yl)ethan-1-ol (NEU-1053) has recently been identified from a high-throughput screen of >42,000 compounds as a highly potent and fast-acting trypanocidal agent capable of curing a bloodstream infection of Trypanosoma brucei in mice. We have designed a library of analogues to probe the structure-activity relationship and improve the predicted central nervous system (CNS) exposure of NEU-1053. We report the activity of these inhibitors of T. brucei, the efficacy of NEU-1053 in a murine CNS model of infection, and identification of the target of NEU-1053 via X-ray crystallography.

Synthesis of Unsymmetrical Diheteroarylbenzenes: Benzoazole and Quinazoline Derivatives

Garin, Javier,Melendez, Enrique,Merchan, Francisco L.,Merino, Pedro,Orduna, Jesus,Tejero, Tomas

, p. 359 - 363 (2007/10/02)

Four different types of structures, namely 8, 14, 17 and 18 have been prepared for the first time.No more than five steps are needed to synthesize them using 4-nitroaniline as starting material.In order to confirm the proposed structures, some independent

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