(3-Bromo-4-fluorophenyl)(morpholino)methanone
97%
- Product Code: 113197
CAS:
1007207-89-7
Molecular Weight: | 288.11 g./mol | Molecular Formula: | C₁₁H₁₁BrFNO₂ |
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EC Number: | MDL Number: | MFCD11053798 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both bromo and fluoro substituents, makes it valuable for developing compounds with potential therapeutic properties, particularly in the design of kinase inhibitors and other enzyme-targeting drugs. Additionally, the morpholine ring in its structure enhances its ability to interact with biological targets, making it a useful building block in drug discovery efforts aimed at treating diseases such as cancer, inflammation, and neurological disorders. Researchers also explore its applications in creating novel compounds for studying biochemical pathways and drug mechanisms.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $60.44 |
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5.000 | 10-20 days | $211.34 |
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25.000 | 10-20 days | $738.84 |
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(3-Bromo-4-fluorophenyl)(morpholino)methanone
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both bromo and fluoro substituents, makes it valuable for developing compounds with potential therapeutic properties, particularly in the design of kinase inhibitors and other enzyme-targeting drugs. Additionally, the morpholine ring in its structure enhances its ability to interact with biological targets, making it a useful building block in drug discovery efforts aimed at treating diseases such as cancer, inflammation, and neurological disorders. Researchers also explore its applications in creating novel compounds for studying biochemical pathways and drug mechanisms.
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