Morpholino(1H-pyrazol-4-yl)methanone
97%
- Product Code: 122382
CAS:
1152749-21-7
| Molecular Weight: | 181.19 g./mol | Molecular Formula: | C₈H₁₁N₃O₂ |
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| EC Number: | MDL Number: | MFCD12142788 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Morpholino(1H-pyrazol-4-yl)methanone finds its primary application in the field of medicinal chemistry, where it is utilized as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring both morpholine and pyrazole moieties, makes it a versatile building block for designing molecules with potential therapeutic properties. It is often employed in the development of small molecule inhibitors targeting specific enzymes or receptors, particularly in the context of cancer research, inflammation, and infectious diseases. Additionally, it is explored in the creation of novel heterocyclic compounds for drug discovery programs, where its unique chemical framework can enhance binding affinity and pharmacokinetic properties. Researchers also leverage its reactivity in organic synthesis to construct complex molecular architectures for further biological evaluation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,354.00 |
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| 0.250 | 10-20 days | ฿9,531.00 |
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| 1.000 | 10-20 days | ฿23,814.00 |
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Morpholino(1H-pyrazol-4-yl)methanone
Morpholino(1H-pyrazol-4-yl)methanone finds its primary application in the field of medicinal chemistry, where it is utilized as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring both morpholine and pyrazole moieties, makes it a versatile building block for designing molecules with potential therapeutic properties. It is often employed in the development of small molecule inhibitors targeting specific enzymes or receptors, particularly in the context of cancer research, inflammation, and infectious diseases. Additionally, it is explored in the creation of novel heterocyclic compounds for drug discovery programs, where its unique chemical framework can enhance binding affinity and pharmacokinetic properties. Researchers also leverage its reactivity in organic synthesis to construct complex molecular architectures for further biological evaluation.
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