4-Bromo-5-methyl-1H-pyrazole-3-carboxylic acid
95%
- Product Code: 86807
CAS:
82231-52-5
| Molecular Weight: | 205.01 g./mol | Molecular Formula: | C₅H₅BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08056671 | |
| Melting Point: | 273-276 °C | Boiling Point: | 410.8±45.0 °C(Predicted) |
| Density: | 1.934±0.06 g/cm3(Predicted) | Storage Condition: | room temperature, inert atmosphere |
Product Description:
This compound is primarily utilized in the synthesis of various pharmaceutical intermediates and active pharmaceutical ingredients (APIs). It serves as a key building block in the development of compounds with potential biological activities, such as anti-inflammatory, antimicrobial, and anticancer agents. Its pyrazole core structure is particularly valuable in medicinal chemistry for designing molecules that interact with specific biological targets. Additionally, it is employed in the preparation of agrochemicals, contributing to the development of pesticides and herbicides. The bromine and carboxylic acid functional groups make it a versatile reagent for further chemical modifications, enabling the creation of diverse derivatives for research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,547.00 |
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| 1.000 | 10-20 days | ฿6,516.00 |
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| 5.000 | 10-20 days | ฿22,698.00 |
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4-Bromo-5-methyl-1H-pyrazole-3-carboxylic acid
This compound is primarily utilized in the synthesis of various pharmaceutical intermediates and active pharmaceutical ingredients (APIs). It serves as a key building block in the development of compounds with potential biological activities, such as anti-inflammatory, antimicrobial, and anticancer agents. Its pyrazole core structure is particularly valuable in medicinal chemistry for designing molecules that interact with specific biological targets. Additionally, it is employed in the preparation of agrochemicals, contributing to the development of pesticides and herbicides. The bromine and carboxylic acid functional groups make it a versatile reagent for further chemical modifications, enabling the creation of diverse derivatives for research and industrial applications.
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