(tert-Butoxycarbonylmethyl)triphenylphosphonium chloride
98%
- Product Code: 76736
CAS:
35000-37-4
| Molecular Weight: | 412.89 g./mol | Molecular Formula: | C₂₄H₂₆ClO₂P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00043160 | |
| Melting Point: | 191-193°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, stored in argon |
Product Description:
This chemical is primarily used in organic synthesis as a reagent for the preparation of protected amino acids and peptides. It facilitates the introduction of the tert-butoxycarbonyl (Boc) protecting group, which is crucial in peptide synthesis to shield amino groups during reactions. The compound is also employed in the synthesis of phosphonium salts, which are valuable intermediates in various organic transformations, including the Wittig reaction. Additionally, it finds application in the development of pharmaceuticals and bioactive molecules, where selective protection and deprotection of functional groups are essential. Its role in enabling efficient and controlled synthetic pathways makes it a valuable tool in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,431.00 |
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| 25.000 | 10-20 days | ฿4,320.00 |
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| 100.000 | 10-20 days | ฿15,219.00 |
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(tert-Butoxycarbonylmethyl)triphenylphosphonium chloride
This chemical is primarily used in organic synthesis as a reagent for the preparation of protected amino acids and peptides. It facilitates the introduction of the tert-butoxycarbonyl (Boc) protecting group, which is crucial in peptide synthesis to shield amino groups during reactions. The compound is also employed in the synthesis of phosphonium salts, which are valuable intermediates in various organic transformations, including the Wittig reaction. Additionally, it finds application in the development of pharmaceuticals and bioactive molecules, where selective protection and deprotection of functional groups are essential. Its role in enabling efficient and controlled synthetic pathways makes it a valuable tool in medicinal chemistry and drug discovery.
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