Cas no 69984-77-6 (1H-Benzimidazol-4-amine)

1H-Benzimidazol-4-amine is a heterocyclic organic compound featuring a benzimidazole core with an amine functional group at the 4-position. This structure imparts significant versatility in pharmaceutical and agrochemical applications, serving as a key intermediate in the synthesis of bioactive molecules. Its aromatic amine moiety enhances reactivity, enabling facile derivatization for the development of inhibitors, ligands, and other specialized compounds. The compound's stability and well-defined reactivity profile make it suitable for use in medicinal chemistry research, particularly in the design of antitumor, antimicrobial, and antiviral agents. High purity grades are available to ensure consistency in synthetic workflows.
1H-Benzimidazol-4-amine structure
1H-Benzimidazol-4-amine structure
Product Name:1H-Benzimidazol-4-amine
CAS No:69984-77-6
MF:C7H7N3
MW:133.150580644608
CID:853178
PubChem ID:20329
Update Time:2025-10-28

1H-Benzimidazol-4-amine Chemical and Physical Properties

Names and Identifiers

    • 1H-Benzimidazol-7-amine(9CI)
    • 1H-benzimidazol-7-amine
    • 1H-Benzimidazol-4-amine
    • 4-Aminobenzimidazole
    • 1H-BENZO[D]IMIDAZOL-7-AMINE
    • 1H-benzo[d]imidazol-4-amine
    • 1H-1,3-benzodiazol-4-amine
    • BENZIMIDAZOLE, 4-AMINO-
    • 1H-Benzimidazole-4-amine
    • 4-Amino-1H-benzimidazole
    • 3H-BENZO[D]IMIDAZOL-4-AMINE
    • 7-Aminobenzimidazole
    • 1H-benzimidazol-4-ylamine
    • 4I33QGV1TN
    • benzimidazole-4-ylamine
    • 4-AMINOBENZIMIDAZOLE HCL
    • NSC143985
    • PubChem8065
    • 4(7)-Aminobenzimidazole
    • 7-Amino-1H-benzimidazole
    • 1H-benzo
    • A6986
    • DTXSID20195821
    • CS-W006218
    • 69984-77-6
    • BCP32844
    • 4331-29-7
    • NCGC00184184-01
    • SB22907
    • AM85770
    • SY025999
    • FT-0647119
    • EN300-58070
    • 1H-benzoimidazol-4-ylamine
    • BB 0260290
    • MFCD01658254
    • AT-051/40231700
    • NSC 143985
    • 7WA
    • SCHEMBL312427
    • BENZIMIDAZOL-4-YLAMINE
    • J-512585
    • AKOS015890340
    • NSC-143985
    • EU-0020139
    • 1H-benzoimidazol-4-yl-amine
    • BS-13308
    • NZJKEQFPRPAEPO-UHFFFAOYSA-N
    • AKOS005171772
    • 1H-benzo[d]imidazol-4-amine;4-Aminobenzimidazole
    • P10197
    • 1H-benzo[d]imidazol-4-amine;1H-Benzo[d]imidazol-7-amine
    • Benzimidazole, 4(or 7)-amino-
    • UNII-4I33QGV1TN
    • Z1259162108
    • STK505486
    • Inchi: 1S/C7H7N3/c8-5-2-1-3-6-7(5)10-4-9-6/h1-4H,8H2,(H,9,10)
    • InChI Key: NZJKEQFPRPAEPO-UHFFFAOYSA-N
    • SMILES: N1C=NC2C(=CC=CC1=2)N

Computed Properties

  • Exact Mass: 133.063997236g/mol
  • Monoisotopic Mass: 133.063997236g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 126
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 54.7
  • XLogP3: 0.8

1H-Benzimidazol-4-amine Pricemore >>

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Additional information on 1H-Benzimidazol-4-amine

1H-Benzimidazol-4-amine: A Comprehensive Overview

1H-Benzimidazol-4-amine (CAS No: 69984-77-6) is a versatile heterocyclic compound that has garnered significant attention in various fields of chemistry and materials science. This compound, with its unique structural features, has been extensively studied for its potential applications in drug design, sensor technology, and advanced materials. The benzimidazole core of the molecule provides a rigid and aromatic framework, while the amine group at the 4-position introduces functional versatility, making it a valuable building block in organic synthesis.

Recent advancements in synthetic methodologies have enabled the efficient preparation of 1H-Benzimidazol-4-amine and its derivatives. Researchers have explored various routes, including condensation reactions and transition-metal-catalyzed coupling processes, to synthesize this compound with high yields and purity. These methods not only enhance the scalability of production but also pave the way for the creation of more complex architectures incorporating the benzimidazole moiety.

The electronic properties of 1H-Benzimidazol-4-amine make it an attractive candidate for applications in optoelectronics and sensing technologies. Studies have demonstrated that this compound exhibits excellent charge transport characteristics, which are crucial for devices such as organic light-emitting diodes (OLEDs) and field-effect transistors (FETs). Furthermore, its ability to form stable complexes with metal ions has led to its use in designing sensors for heavy metal ions, such as lead (Pb2?) and mercury (Hg2?), which are critical for environmental monitoring.

In the realm of drug discovery, 1H-Benzimidazol-4-amine has shown promise as a scaffold for developing bioactive molecules. Its structural flexibility allows for the incorporation of various substituents that can modulate pharmacokinetic properties and target specific biological pathways. Recent research has focused on its potential as an anticancer agent, where it has been found to exhibit selective cytotoxicity against cancer cells while sparing normal cells. Additionally, derivatives of this compound have been investigated for their anti-inflammatory and antioxidant activities, further highlighting its therapeutic potential.

The integration of 1H-Benzimidazol-4-amine into polymer systems has opened new avenues for materials science applications. By incorporating this compound into polymeric matrices, researchers have developed materials with enhanced mechanical strength and thermal stability. These materials find applications in high-performance composites and advanced coatings, where durability and resistance to environmental factors are paramount.

From a sustainability perspective, the synthesis and application of 1H-Benzimidazol-4-amine align with green chemistry principles. The development of eco-friendly synthetic routes and the use of renewable feedstocks have reduced the environmental footprint associated with its production. Moreover, its application in energy-efficient devices contributes to reducing overall energy consumption in various industries.

In conclusion, 1H-Benzimidazol-4-amine (CAS No: 69984-77-6) stands as a testament to the ingenuity of modern chemical research. Its unique combination of structural features, functional versatility, and compatibility with advanced synthetic techniques positions it as a key player in diverse scientific domains. As research continues to uncover new applications and optimize existing ones, this compound is poised to make significant contributions to both academic advancements and industrial innovations.

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