4,6-Dihydro-1H-pyrrolo[3,4-c]pyrazole-5-carboxylic acid benzyl ester
≥95%
- Product Code: 45911
CAS:
1440526-39-5
| Molecular Weight: | 243.265 g./mol | Molecular Formula: | C₁₃H₁₃N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 465.8±45.0 °C | |
| Density: | 1.355±0.06 g/cm3 | Storage Condition: | room temperature |
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 a pyrrolopyrazole core, makes it a valuable building block for developing compounds with potential therapeutic applications. Researchers often employ it in the design and synthesis of inhibitors targeting specific enzymes or receptors, particularly in the context of drug discovery for diseases such as cancer, inflammation, and neurological disorders. Additionally, its benzyl ester group enhances its reactivity, facilitating further chemical modifications to optimize pharmacological properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light Yellow Powder |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $163.16 |
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| 1.000 | 10-20 days | $703.54 |
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| 5.000 | 10-20 days | $1,656.41 |
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4,6-Dihydro-1H-pyrrolo[3,4-c]pyrazole-5-carboxylic acid benzyl ester
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 a pyrrolopyrazole core, makes it a valuable building block for developing compounds with potential therapeutic applications. Researchers often employ it in the design and synthesis of inhibitors targeting specific enzymes or receptors, particularly in the context of drug discovery for diseases such as cancer, inflammation, and neurological disorders. Additionally, its benzyl ester group enhances its reactivity, facilitating further chemical modifications to optimize pharmacological properties.
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