2-(3-Aminophenyl)-1H-benzo[d]imidazol-6-amine
95%
- Product Code: 115685
CAS:
13676-49-8
Molecular Weight: | 224.26 g./mol | Molecular Formula: | C₁₃H₁₂N₄ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 562.7°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical agents. Its structure, featuring both amino and benzimidazole groups, makes it particularly valuable in the development of drugs targeting specific biological pathways.
In medicinal chemistry, it is often employed in the synthesis of compounds with potential anticancer, antimicrobial, and anti-inflammatory properties. The presence of the benzimidazole moiety allows it to interact with biological targets such as enzymes and receptors, making it a versatile building block for drug discovery.
Additionally, this chemical is explored in the development of dyes and pigments due to its ability to form stable, colored complexes. Its application extends to materials science, where it is investigated for its potential in creating advanced polymers and coatings with enhanced performance characteristics.
Overall, its multifunctional nature makes it a valuable component in both industrial and research settings, contributing to advancements in healthcare, materials, and chemical manufacturing.
Product Specification:
Test | Specification |
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Appearance | White To Light-Yellow Powder Or Crystals |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $52.74 |
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1.000 | 10-20 days | $126.25 |
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2-(3-Aminophenyl)-1H-benzo[d]imidazol-6-amine
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical agents. Its structure, featuring both amino and benzimidazole groups, makes it particularly valuable in the development of drugs targeting specific biological pathways.
In medicinal chemistry, it is often employed in the synthesis of compounds with potential anticancer, antimicrobial, and anti-inflammatory properties. The presence of the benzimidazole moiety allows it to interact with biological targets such as enzymes and receptors, making it a versatile building block for drug discovery.
Additionally, this chemical is explored in the development of dyes and pigments due to its ability to form stable, colored complexes. Its application extends to materials science, where it is investigated for its potential in creating advanced polymers and coatings with enhanced performance characteristics.
Overall, its multifunctional nature makes it a valuable component in both industrial and research settings, contributing to advancements in healthcare, materials, and chemical manufacturing.
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