2-((2-Bromo-1,1,2,2-tetrafluoroethyl)thio)pyridine
97%
- Product Code: 123971
CAS:
1000293-89-9
Molecular Weight: | 290.08 g./mol | Molecular Formula: | C₇H₄BrF₄NS |
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EC Number: | MDL Number: | MFCD31618523 | |
Melting Point: | Boiling Point: | 198.7±40.0 °C(Predicted) | |
Density: | 1.75±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry, dark |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a bromo-tetrafluoroethyl group attached to a pyridine ring, makes it a valuable intermediate for introducing fluorine-containing moieties into more complex molecules. Fluorinated compounds are often sought after in drug discovery due to their enhanced stability, bioavailability, and metabolic resistance. Additionally, this chemical can be employed in the synthesis of sulfur-containing heterocycles, which are important in the creation of biologically active compounds. Its reactivity with nucleophiles also makes it useful in cross-coupling reactions, enabling the construction of diverse molecular architectures.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,592.00 |
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0.250 | 10-20 days | ฿3,879.00 |
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1.000 | 10-20 days | ฿9,684.00 |
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2-((2-Bromo-1,1,2,2-tetrafluoroethyl)thio)pyridine
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a bromo-tetrafluoroethyl group attached to a pyridine ring, makes it a valuable intermediate for introducing fluorine-containing moieties into more complex molecules. Fluorinated compounds are often sought after in drug discovery due to their enhanced stability, bioavailability, and metabolic resistance. Additionally, this chemical can be employed in the synthesis of sulfur-containing heterocycles, which are important in the creation of biologically active compounds. Its reactivity with nucleophiles also makes it useful in cross-coupling reactions, enabling the construction of diverse molecular architectures.
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