((4-(4-Fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)methyl)triphenylphosphonium bromide
≥98%
- Product Code: 46287
CAS:
877997-99-4
| Molecular Weight: | 338.33576 g./mol | Molecular Formula: | C₁₄H₁₄N₂O₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26127250 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, airtight, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile reagent for the introduction of functional groups or as a key intermediate in the preparation of complex molecules. Its structure, featuring a triphenylphosphonium moiety, makes it particularly useful in Wittig reactions, where it facilitates the formation of alkenes from carbonyl compounds. Additionally, the presence of the sulfonamido group enhances its stability and reactivity, making it suitable for use in medicinal chemistry for the development of biologically active compounds. Its fluorophenyl group can contribute to interactions with biological targets, potentially aiding in drug discovery efforts. Overall, it serves as a valuable tool in both synthetic organic chemistry and pharmaceutical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿468.00 |
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| 5.000 | 10-20 days | ฿1,431.00 |
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| 25.000 | 10-20 days | ฿4,482.00 |
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((4-(4-Fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)methyl)triphenylphosphonium bromide
This compound is primarily utilized in organic synthesis as a versatile reagent for the introduction of functional groups or as a key intermediate in the preparation of complex molecules. Its structure, featuring a triphenylphosphonium moiety, makes it particularly useful in Wittig reactions, where it facilitates the formation of alkenes from carbonyl compounds. Additionally, the presence of the sulfonamido group enhances its stability and reactivity, making it suitable for use in medicinal chemistry for the development of biologically active compounds. Its fluorophenyl group can contribute to interactions with biological targets, potentially aiding in drug discovery efforts. Overall, it serves as a valuable tool in both synthetic organic chemistry and pharmaceutical research.
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