N-(Tert-butoxycarbonylamino)phthalimide
95%
- Product Code: 80161
CAS:
34387-89-8
| Molecular Weight: | 262.26 g./mol | Molecular Formula: | C₁₃H₁₄N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00686624 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily used in organic synthesis as a protecting group for amines. It is particularly effective in peptide synthesis, where it safeguards the amino group during reactions involving other functional groups. The tert-butoxycarbonyl (Boc) group can be easily removed under acidic conditions, allowing for the controlled deprotection of the amine when needed. Additionally, it finds application in the preparation of pharmaceuticals and agrochemicals, where selective protection of amines is crucial for the synthesis of complex molecules. Its stability under basic conditions and compatibility with various reaction conditions make it a versatile reagent in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿693.00 |
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| 5.000 | 10-20 days | ฿2,493.00 |
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| 25.000 | 10-20 days | ฿8,739.00 |
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N-(Tert-butoxycarbonylamino)phthalimide
This compound is primarily used in organic synthesis as a protecting group for amines. It is particularly effective in peptide synthesis, where it safeguards the amino group during reactions involving other functional groups. The tert-butoxycarbonyl (Boc) group can be easily removed under acidic conditions, allowing for the controlled deprotection of the amine when needed. Additionally, it finds application in the preparation of pharmaceuticals and agrochemicals, where selective protection of amines is crucial for the synthesis of complex molecules. Its stability under basic conditions and compatibility with various reaction conditions make it a versatile reagent in synthetic chemistry.
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