3-Amino-7-chloro-5-nitro-1H-indazole
≥95%
- Product Code: 69511
CAS:
1197193-46-6
| Molecular Weight: | 212.59 g./mol | Molecular Formula: | C₇H₅ClN₄O₂ |
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| EC Number: | MDL Number: | MFCD07385614 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
3-Amino-7-chloro-5-nitro-1H-indazole is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of various heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers leverage this chemical in the creation of novel drug candidates, particularly in the search for new therapeutic agents with anti-inflammatory, antimicrobial, or anticancer properties. Additionally, it serves as a building block in the preparation of dyes and pigments, contributing to advancements in material science and industrial applications. Its unique chemical properties also make it a subject of interest in academic research for studying reaction mechanisms and developing new synthetic methodologies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $143.08 |
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| 1g | 10-20 days | $349.12 |
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3-Amino-7-chloro-5-nitro-1H-indazole
3-Amino-7-chloro-5-nitro-1H-indazole is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of various heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers leverage this chemical in the creation of novel drug candidates, particularly in the search for new therapeutic agents with anti-inflammatory, antimicrobial, or anticancer properties. Additionally, it serves as a building block in the preparation of dyes and pigments, contributing to advancements in material science and industrial applications. Its unique chemical properties also make it a subject of interest in academic research for studying reaction mechanisms and developing new synthetic methodologies.
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