Methyl 1,2-dihydro-1-methyl-2-oxopyridine-5-carboxylate
97%
- Product Code: 126362
CAS:
6375-89-9
| Molecular Weight: | 167.16 g./mol | Molecular Formula: | C8H9NO3 |
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| EC Number: | MDL Number: | MFCD00031001 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its structure allows it to participate in reactions that form more complex molecules, particularly those with pyridine rings, which are common in drug design. It is often employed in the development of compounds with potential therapeutic properties, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, its reactivity makes it useful in the synthesis of fine chemicals and specialty materials, where precise molecular modifications are required. Its application extends to research laboratories, where it serves as a building block for exploring new chemical reactions and pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $56.06 |
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| 5.000 | 10-20 days | $246.27 |
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| 25.000 | 10-20 days | $1,193.13 |
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Methyl 1,2-dihydro-1-methyl-2-oxopyridine-5-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its structure allows it to participate in reactions that form more complex molecules, particularly those with pyridine rings, which are common in drug design. It is often employed in the development of compounds with potential therapeutic properties, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, its reactivity makes it useful in the synthesis of fine chemicals and specialty materials, where precise molecular modifications are required. Its application extends to research laboratories, where it serves as a building block for exploring new chemical reactions and pathways.
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