3-Amino-1-methyl-5-(methylthio)-1H-pyrazole-4-carbonitrile
95%
- Product Code: 81093
CAS:
151291-05-3
| Molecular Weight: | 168.22 g./mol | Molecular Formula: | C₆H₈N₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02089753 | |
| Melting Point: | 120 °C | Boiling Point: | 386.1±42.0 °C(Predicted) |
| Density: | 1.37±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of various pharmaceutical compounds due to its unique structure, which allows it to act as a key intermediate in the production of drugs targeting specific biological pathways. It is particularly valuable in the development of molecules with potential anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its pyrazole core makes it a versatile building block in organic chemistry, enabling the creation of complex heterocyclic compounds used in drug discovery and development. Its incorporation into larger molecular frameworks often enhances the bioactivity and specificity of the resulting compounds, making it a crucial component in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $329.69 |
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| 0.250 | 10-20 days | $549.48 |
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| 1.000 | 10-20 days | $1,098.96 |
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3-Amino-1-methyl-5-(methylthio)-1H-pyrazole-4-carbonitrile
This chemical is primarily utilized in the synthesis of various pharmaceutical compounds due to its unique structure, which allows it to act as a key intermediate in the production of drugs targeting specific biological pathways. It is particularly valuable in the development of molecules with potential anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its pyrazole core makes it a versatile building block in organic chemistry, enabling the creation of complex heterocyclic compounds used in drug discovery and development. Its incorporation into larger molecular frameworks often enhances the bioactivity and specificity of the resulting compounds, making it a crucial component in medicinal chemistry research.
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