1-Benzyl-3-(chloromethyl)-1H-indazole
≥97%
- Product Code: 68096
CAS:
131427-22-0
| Molecular Weight: | 256.73 g./mol | Molecular Formula: | C₁₅H₁₃ClN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20134218 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a benzyl group and a chloromethyl group, makes it a versatile building block for the development of potential pharmaceutical agents. It is often employed in the creation of indazole derivatives, which are known for their therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. Additionally, it serves as a precursor in the design of enzyme inhibitors and receptor modulators, contributing to drug discovery and development efforts. Its reactivity allows for further functionalization, enabling researchers to explore a wide range of chemical modifications to optimize biological activity and drug efficacy.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow solid |
| PURITY | 97-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,280.00 |
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| 1.000 | 10-20 days | ฿12,850.00 |
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1-Benzyl-3-(chloromethyl)-1H-indazole
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a benzyl group and a chloromethyl group, makes it a versatile building block for the development of potential pharmaceutical agents. It is often employed in the creation of indazole derivatives, which are known for their therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. Additionally, it serves as a precursor in the design of enzyme inhibitors and receptor modulators, contributing to drug discovery and development efforts. Its reactivity allows for further functionalization, enabling researchers to explore a wide range of chemical modifications to optimize biological activity and drug efficacy.
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