((4-(4-Fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)methyl)triphenylphosphonium bromide
98%
- Product Code: 52895
CAS:
885477-83-8
| Molecular Weight: | 678.604 g./mol | Molecular Formula: | C₃₄H₃₄BrFN₃O₂PS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12911893 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
This compound is primarily used in organic synthesis as a versatile reagent, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrimidine core and a triphenylphosphonium group, makes it valuable in facilitating various chemical reactions, such as nucleophilic substitutions and coupling reactions. It is often employed in the preparation of complex molecules, where its unique reactivity aids in the formation of carbon-carbon or carbon-heteroatom bonds. Additionally, its fluorophenyl and sulfonamido groups contribute to its utility in designing biologically active compounds, potentially targeting enzymes or receptors in drug discovery. Its application extends to materials science, where it can be used in the synthesis of advanced polymers or functional materials.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿750.00 |
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| 25.000 | 10-20 days | ฿2,610.00 |
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| 100.000 | 10-20 days | ฿8,330.00 |
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((4-(4-Fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)methyl)triphenylphosphonium bromide
This compound is primarily used in organic synthesis as a versatile reagent, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrimidine core and a triphenylphosphonium group, makes it valuable in facilitating various chemical reactions, such as nucleophilic substitutions and coupling reactions. It is often employed in the preparation of complex molecules, where its unique reactivity aids in the formation of carbon-carbon or carbon-heteroatom bonds. Additionally, its fluorophenyl and sulfonamido groups contribute to its utility in designing biologically active compounds, potentially targeting enzymes or receptors in drug discovery. Its application extends to materials science, where it can be used in the synthesis of advanced polymers or functional materials.
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