N-BOC-IMINO-(TRIPHENYL)PHOSPHORANE
98%
- Product Code: 60093
Alias:
N-tert-butoxycarbonylimine(triphenyl)phosphineN-BOC-iminotriphenylphosphineN-BOC-iminotriphenylphosphinetriphenylphosphinoiminocarbamate tert-butyl esterN-BOC- Triphenylphosphorimide N-BOC-triphenylphosphorimide
CAS:
68014-21-1
Molecular Weight: | 377.42 g./mol | Molecular Formula: | C₂₃H₂₄NO₂P |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the preparation of protected amino acids and peptides. It serves as a key reagent in the formation of imines and other nitrogen-containing compounds, facilitating the introduction of the BOC (tert-butoxycarbonyl) protecting group. This protecting group is crucial in peptide synthesis as it shields the amine functionality during reactions, allowing selective deprotection at a later stage. The compound is also employed in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where precise control over nitrogen-based functional groups is required. Its stability and reactivity make it a valuable tool in the development of novel chemical entities and in the modification of biomolecules.
Product Specification:
Test | Specification |
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Purity | 98 100% |
APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
Proton NMR Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿290.00 |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿520.00 |
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N-BOC-IMINO-(TRIPHENYL)PHOSPHORANE
This chemical is primarily used in organic synthesis, particularly in the preparation of protected amino acids and peptides. It serves as a key reagent in the formation of imines and other nitrogen-containing compounds, facilitating the introduction of the BOC (tert-butoxycarbonyl) protecting group. This protecting group is crucial in peptide synthesis as it shields the amine functionality during reactions, allowing selective deprotection at a later stage. The compound is also employed in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where precise control over nitrogen-based functional groups is required. Its stability and reactivity make it a valuable tool in the development of novel chemical entities and in the modification of biomolecules.
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