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1-phenyl-3-naphthalen-1-ylmethylbenzimidazolium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1574707-44-0 Structure
  • Basic information

    1. Product Name: 1-phenyl-3-naphthalen-1-ylmethylbenzimidazolium chloride
    2. Synonyms: 1-phenyl-3-naphthalen-1-ylmethylbenzimidazolium chloride
    3. CAS NO:1574707-44-0
    4. Molecular Formula:
    5. Molecular Weight: 370.881
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1574707-44-0.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: 1-phenyl-3-naphthalen-1-ylmethylbenzimidazolium chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-3-naphthalen-1-ylmethylbenzimidazolium chloride(1574707-44-0)
    11. EPA Substance Registry System: 1-phenyl-3-naphthalen-1-ylmethylbenzimidazolium chloride(1574707-44-0)
  • 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: 1574707-44-0(Hazardous Substances Data)

1574707-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1574707-44-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,4,7,0 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1574707-44:
(9*1)+(8*5)+(7*7)+(6*4)+(5*7)+(4*0)+(3*7)+(2*4)+(1*4)=190
190 % 10 = 0
So 1574707-44-0 is a valid CAS Registry Number.

1574707-44-0Downstream Products

1574707-44-0Relevant articles and documents

Carbon-carbon bond formation catalyzed by PEPPSI Pd-NHC

Akko?, Senem,?zer ?lhan, ?lhan,G?k, Yetkin,Kayser, Veysel

, p. 52 - 56 (2017)

Five new palladium complexes were efficiently synthesized from the reaction of benzimidazolium salts, potassium carbonate (K2CO3) and palladium chloride (PdCl2) in pyridine (for 3–5) or 3-chloropyridine (for 6 and 7). The synthesized complexes were characterized and tested in Suzuki-Miyaura cross-coupling reaction as catalysts. In the presence of catalysts 3–7, biaryl products were obtained in moderate yields when phenylboronic acid was used as boronic acid derivative. However, the coupling of thianaphthene-2-boronic acid with 1-chloro-4-nitrobenzene generated low yields although a longer period of time was used in comparison to the coupling of phenylboronic acid with aryl chlorides.

N-Phenyl-substituted carbene precursors and their silver complexes: Synthesis, characterization and antimicrobial activities

Goek, Yetkin,Akkoc, Senem,Albayrak, Sevil,Akkurt, Mehmet,Tahir, Muhammad Nawaz

, p. 244 - 251 (2014/04/03)

A series of unsymmetrically substituted N-heterocyclic carbene (NHC) precursors (1a, 1b, 1c, 1d, 1e) were synthesized from the reaction of N-phenylbenzimidazole with various alkyl halides. These compounds were used to synthesize NHC-silver(I) complexes (2a, 2b, 2c, 2d, 2e). The five new 1-phenyl-3-alkylbenzimidazolium salts (1a, 1b, 1c, 1d, 1e) and their NHC-silver complexes (2a, 2b, 2c, 2d, 2e) were characterized by the 1H NMR, 13C NMR and FT-IR spectroscopic methods and elemental analysis techniques. Also, the two NHC-silver complexes 2b and 2c were characterized by single-crystal X-ray crystallography, which confirmed the linear C - Ag - Cl arrangements. The antibacterial activities of the NHC precursor and NHC-silver complexes were tested against three Gram-positive bacterial strains (Bacillus subtilis, Listeria monocytogenes and Staphylococcus aureus) and three Gram-negative bacterial strains (Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa) using the microdilution broth method. The NHC-silver complexes showed higher antibacterial activity than the NHC precursors. In addition, silver complexes 2a, 2b, 2c, 2d showed high antibacterial activity against the Gram-positive bacteria L. monocytogenes and S. aureus compared to the standard, tetracycline. Copyright

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