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2562-73-4

Benzenamine, N,N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl)-, also known as N,N-dimethyl-4-(1-phenylbenzimidazol-2-yl)aniline, is a complex organic compound with the molecular formula C21H20N4. It is a derivative of benzenamine (aniline), featuring a benzimidazole ring attached to the para position of the aniline group. Benzenamine, N,N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl)- is characterized by its unique molecular structure, which consists of a benzene ring with two nitrogen atoms (forming the benzimidazole) and two methyl groups attached to the nitrogen of the aniline. It is a white to off-white crystalline solid and is used in various chemical and pharmaceutical applications, such as the synthesis of dyes, pigments, and pharmaceuticals. Due to its complex structure, it is important to handle Benzenamine, N,N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl)- with care, following proper safety protocols.

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  • 2562-73-4 Structure

  • Basic information

    1. Product Name: Benzenamine, N,N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl)-
    2. Synonyms:
    3. CAS NO:2562-73-4
    4. Molecular Formula: C21H19N3
    5. Molecular Weight: 313.402
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2562-73-4.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: Benzenamine, N,N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenamine, N,N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl)-(2562-73-4)
    11. EPA Substance Registry System: Benzenamine, N,N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl)-(2562-73-4)

  • 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: 2562-73-4(Hazardous Substances Data)

2562-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2562-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2562-73:
(6*2)+(5*5)+(4*6)+(3*2)+(2*7)+(1*3)=84
84 % 10 = 4
So 2562-73-4 is a valid CAS Registry Number.

2562-73-4Downstream Products

2562-73-4Relevant articles and documents

Novel Benzimidazole- Platinum(II) Complexes: Synthesis, Characterization, Antimicrobial and Anticancer Activity

?zcan, ?zge,?ri?li, Sevil,?ahin, Onur,Alaca, Gizem,Ar?, Aydan,Do?an, Umut,Günnaz, Salih,Yal??n, H. Tansel

, (2021/01/11)

Three new Platinum complexes (1-3) with 2,6-di-tert-butyl-4-(1-phenyl-1H-benzimidazol-2-yl) phenol (L1), N, N-dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl) aniline (L2) and 4-(1H-benzimidazol-2-yl)-N, N-dimethylaniline (L3) w

Benzimidazoles: A new class of carbonic anhydrase inhibitors

Khan, Khalid Mohammed,Khan, Momin,Saleem, Muhammad,Taha, Muhammad,Perveen, Shahnaz,Choudhary, Mohammad Iqbal

, p. 901 - 904 (2013/07/26)

Carbonic anhydrase inhibitory activity of benzimidazole derivatives 1-24 has been evaluated. Compounds 22 (IC50 = 7.47 ± 0.39 μM), 21 (IC50 = 10.31 ± 0.11 μM), 20 (IC50 = 23.1 ± 1.78 μM), 12 (IC50 = 12.16 ± 0.10

Conventional and microwave-assisted synthesis of benzimidazole derivatives and their in vitro inhibition of human cyclooxygenase

Secci, Daniela,Bolasco, Adriana,D'Ascenzio, Melissa,Della Sala, Flavio,Yanez, Matilde,Carradori, Simone

, p. 1187 - 1195 (2013/01/15)

A large series of 1,2-diaryl-benzimidazole and 2-aryl-1H-benzimidazole derivatives were synthesized with slight differences using both microwave irradiation and conventional heating methods. Usually higher yields and time reactions reduction were obtained

Regiospecific synthesis of 1, 2-disubstituted (hetero)aryl fused imidazoles with tunable fluorescent emission

Zhao, Dongbing,Hu, Junyi,Wu, Ningjie,Huang, Xiaolei,Qin, Xurong,Lan, Jingbo,You, Jingsong

, p. 6516 - 6519 (2012/02/02)

A palladium-catalyzed two or fourfold amination was established that allows regiospecific synthesis of a diversity-oriented library of 1, 2 disubstituted (hetero)aryl fused imidazoles, and provides an exceptional tool for the discovery of fluorescent scaf

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