5-((tert-Butoxycarbonyl)amino)pentyl 4-methylbenzenesulfonate
97%
- Product Code: 84046
CAS:
113080-34-0
Molecular Weight: | 357.47 g./mol | Molecular Formula: | C₁₇H₂₇NO₅S |
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EC Number: | MDL Number: | MFCD07776967 | |
Melting Point: | 47-49 °C | Boiling Point: | |
Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a protected intermediate for the introduction of amino functionalities into more complex molecules. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, preventing unwanted reactions during synthetic processes. The tosyl (4-methylbenzenesulfonate) group is a good leaving group, facilitating nucleophilic substitution reactions. This compound is often employed in peptide synthesis, where the Boc group protects the amino group, and the tosyl group allows for further functionalization or coupling with other molecules. Its stability and reactivity make it a valuable tool in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿972.00 |
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1.000 | 10-20 days | ฿2,430.00 |
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5.000 | 10-20 days | ฿8,478.00 |
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5-((tert-Butoxycarbonyl)amino)pentyl 4-methylbenzenesulfonate
This chemical is primarily utilized in organic synthesis as a protected intermediate for the introduction of amino functionalities into more complex molecules. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, preventing unwanted reactions during synthetic processes. The tosyl (4-methylbenzenesulfonate) group is a good leaving group, facilitating nucleophilic substitution reactions. This compound is often employed in peptide synthesis, where the Boc group protects the amino group, and the tosyl group allows for further functionalization or coupling with other molecules. Its stability and reactivity make it a valuable tool in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.
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