2-BROMO-6-(2,2,2-TRIFLUOROETHOXY)PYRIDINE
95%
- Product Code: 42141
CAS:
869640-44-8
| Molecular Weight: | 256.0199096 g./mol | Molecular Formula: | C₇H₅BrF₃NO |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a versatile intermediate in the synthesis of more complex molecules. Its unique structure, featuring a bromine atom and a trifluoroethoxy group on a pyridine ring, makes it valuable for constructing biologically active compounds. In drug development, it is often employed to introduce specific functional groups that enhance the pharmacological properties of target molecules, such as improved binding affinity or metabolic stability. Additionally, it serves as a key building block in the creation of agrochemicals, where it contributes to the development of pesticides or herbicides with enhanced efficacy and selectivity. Its reactivity also makes it useful in organic synthesis for coupling reactions, enabling the formation of carbon-carbon or carbon-heteroatom bonds in complex chemical processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿15,192.00 |
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| 0.100 | 10-20 days | ฿20,592.00 |
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2-BROMO-6-(2,2,2-TRIFLUOROETHOXY)PYRIDINE
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a versatile intermediate in the synthesis of more complex molecules. Its unique structure, featuring a bromine atom and a trifluoroethoxy group on a pyridine ring, makes it valuable for constructing biologically active compounds. In drug development, it is often employed to introduce specific functional groups that enhance the pharmacological properties of target molecules, such as improved binding affinity or metabolic stability. Additionally, it serves as a key building block in the creation of agrochemicals, where it contributes to the development of pesticides or herbicides with enhanced efficacy and selectivity. Its reactivity also makes it useful in organic synthesis for coupling reactions, enabling the formation of carbon-carbon or carbon-heteroatom bonds in complex chemical processes.
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