4-Iodo-3-methoxy-1H-pyrazole
95%
- Product Code: 47791
CAS:
1350325-05-1
| Molecular Weight: | 223.9998 g./mol | Molecular Formula: | C₄H₅IN₂O |
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| EC Number: | MDL Number: | MFCD27665102 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. It serves as a key intermediate in the preparation of various pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. Additionally, its unique structure makes it valuable in the design of agrochemicals, where it can be incorporated into compounds that exhibit herbicidal or pesticidal properties. Researchers also explore its potential in the development of novel materials, such as organic semiconductors or ligands for catalytic systems, due to its ability to participate in diverse chemical reactions. Its iodine moiety, in particular, allows for further functionalization through cross-coupling reactions, making it a useful tool in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿19,458.00 |
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4-Iodo-3-methoxy-1H-pyrazole
This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. It serves as a key intermediate in the preparation of various pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. Additionally, its unique structure makes it valuable in the design of agrochemicals, where it can be incorporated into compounds that exhibit herbicidal or pesticidal properties. Researchers also explore its potential in the development of novel materials, such as organic semiconductors or ligands for catalytic systems, due to its ability to participate in diverse chemical reactions. Its iodine moiety, in particular, allows for further functionalization through cross-coupling reactions, making it a useful tool in medicinal chemistry and material science.
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