4-Bromo-5-methylpicolinaldehyde
97%
- Product Code: 119353
CAS:
1196157-14-8
Molecular Weight: | 200.03 g./mol | Molecular Formula: | C₇H₆BrNO |
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EC Number: | MDL Number: | MFCD13190304 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
4-Bromo-5-methylpicolinaldehyde is primarily utilized as a key intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both a bromine atom and an aldehyde group, makes it a versatile building block for creating complex molecules. In medicinal chemistry, it is often employed in the development of drug candidates, especially those targeting specific enzymes or receptors. The bromine atom allows for further functionalization through cross-coupling reactions, while the aldehyde group can participate in condensation reactions to form heterocycles or other derivatives. Additionally, it is used in the preparation of ligands for catalysis and in the synthesis of agrochemicals, where it contributes to the creation of compounds with pesticidal or herbicidal properties. Its role in these applications highlights its importance in advancing research and development in chemical sciences.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,528.00 |
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0.250 | 10-20 days | ฿5,643.00 |
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1.000 | 10-20 days | ฿14,130.00 |
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4-Bromo-5-methylpicolinaldehyde
4-Bromo-5-methylpicolinaldehyde is primarily utilized as a key intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both a bromine atom and an aldehyde group, makes it a versatile building block for creating complex molecules. In medicinal chemistry, it is often employed in the development of drug candidates, especially those targeting specific enzymes or receptors. The bromine atom allows for further functionalization through cross-coupling reactions, while the aldehyde group can participate in condensation reactions to form heterocycles or other derivatives. Additionally, it is used in the preparation of ligands for catalysis and in the synthesis of agrochemicals, where it contributes to the creation of compounds with pesticidal or herbicidal properties. Its role in these applications highlights its importance in advancing research and development in chemical sciences.
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