2-Bromo-3-methoxy-6-nitropyridine
≥95%
- Product Code: 116652
CAS:
76066-07-4
| Molecular Weight: | 233.02 g./mol | Molecular Formula: | C₆H₅BrN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06662266 | |
| Melting Point: | Boiling Point: | 364.404°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily used in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique structure, featuring bromine, methoxy, and nitro groups, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is also employed in the preparation of agrochemicals, where it serves as a building block for creating compounds with herbicidal or pesticidal properties. Additionally, its reactivity allows for use in materials science, particularly in the design of advanced organic materials or dyes. Researchers often utilize it in cross-coupling reactions, where it acts as a key reactant to form carbon-carbon or carbon-heteroatom bonds, essential in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,881.00 |
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| 1.000 | 10-20 days | ฿3,834.00 |
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| 5.000 | 10-20 days | ฿11,205.00 |
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| 10.000 | 10-20 days | ฿19,080.00 |
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2-Bromo-3-methoxy-6-nitropyridine
This compound is primarily used in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique structure, featuring bromine, methoxy, and nitro groups, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is also employed in the preparation of agrochemicals, where it serves as a building block for creating compounds with herbicidal or pesticidal properties. Additionally, its reactivity allows for use in materials science, particularly in the design of advanced organic materials or dyes. Researchers often utilize it in cross-coupling reactions, where it acts as a key reactant to form carbon-carbon or carbon-heteroatom bonds, essential in drug discovery and development.
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