6-chloro-2-methyl-2H-indazol-5-amine CAS: 1893125-36-4
Catalog Number | XD93375 |
Product Name | 6-chloro-2-methyl-2H-indazol-5-amine |
CAS | 1893125-36-4 |
Molecular Formula | C8H8ClN3 |
Molecular Weight | 181.62 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
6-Chloro-2-methyl-2H-indazol-5-amine is an organic compound with the chemical formula C8H8ClN3. It belongs to the class of indazoles, which are nitrogen-containing heterocyclic compounds. This particular compound has a chlorine atom at the 6th position, a methyl group at the 2nd position, and an amino group at the 5th position of the indazole ring. It possesses interesting chemical and biological properties, making it useful in various applications.One of the prominent uses of 6-Chloro-2-methyl-2H-indazol-5-amine is in the field of medicinal chemistry. The indazole ring in the molecule is known for its broad-spectrum biological activity. The chlorine atom, methyl group, and amino group present in the compound can be chemically modified to create derivatives with enhanced pharmaceutical properties. These modifications can improve the compound's efficacy, stability, target selectivity, and solubility, making it a potential candidate for drug development.The compound's structural features also make it useful in the field of dye chemistry. The indazole ring system exhibits unique chromophoric properties that can be utilized in the synthesis of dyes and pigments. By introducing different substituents on the indazole ring, chemists can modulate the compound's color and other physical properties, resulting in a wide range of dyes for various applications including textile and ink industries.Furthermore, 6-Chloro-2-methyl-2H-indazol-5-amine offers potential applications in the field of material science. Its diverse reactivity allows it to act as a building block or precursor for the synthesis of functional materials. The compound can be employed in the preparation of organic semiconductors, polymers, and conducting materials. Its ability to undergo chemical modifications enables the creation of materials with tailored electrical, optical, and magnetic properties.In addition, the compound can be used as a highly effective reagent in organic synthesis. It can undergo various reactions, such as nucleophilic substitution, oxidation, and condensation, to form complex organic structures. This versatility enables chemists to explore its use as a key intermediate for the synthesis of pharmaceuticals, agrochemicals, and other useful compounds.In summary, 6-Chloro-2-methyl-2H-indazol-5-amine possesses chemical and biological properties that make it valuable in various applications. Its potential as a drug candidate, dye precursor, and building block for functional materials highlights its versatility in medicinal chemistry, dye chemistry, and material science. Furthermore, its reactivity as a reagent enables its use as an intermediate for the synthesis of diverse organic compounds. Ongoing research and development efforts will likely further uncover its potential in different scientific disciplines.