tert-Butyl 4-(2-ethoxy-1,1-difluoro-2-oxoethyl)-5,6-dihydropyridine-1(2H)-carboxylate
95%
- Product Code: 124248
CAS:
1258637-70-5
Molecular Weight: | 305.32 g./mol | Molecular Formula: | C₁₄H₂₁F₂NO₄ |
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EC Number: | MDL Number: | MFCD18433778 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a difluoro and ethoxy group, makes it valuable for introducing fluorine atoms into target compounds, which can enhance their biological activity and metabolic stability. It is often employed in the development of drugs targeting neurological disorders, cancer, and infectious diseases. Additionally, its dihydropyridine moiety is useful in constructing heterocyclic frameworks, which are common in many bioactive molecules. The tert-butyl group provides steric protection, aiding in selective reactions during multi-step synthetic processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿8,739.00 |
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0.250 | 10-20 days | ฿14,850.00 |
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1.000 | 10-20 days | ฿40,077.00 |
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tert-Butyl 4-(2-ethoxy-1,1-difluoro-2-oxoethyl)-5,6-dihydropyridine-1(2H)-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a difluoro and ethoxy group, makes it valuable for introducing fluorine atoms into target compounds, which can enhance their biological activity and metabolic stability. It is often employed in the development of drugs targeting neurological disorders, cancer, and infectious diseases. Additionally, its dihydropyridine moiety is useful in constructing heterocyclic frameworks, which are common in many bioactive molecules. The tert-butyl group provides steric protection, aiding in selective reactions during multi-step synthetic processes.
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