N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine
95%
- Product Code: 64934
CAS:
153086-78-3
Molecular Weight: | 248.32 g./mol | Molecular Formula: | C₁₁H₂₄N₂O₄ |
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EC Number: | MDL Number: | MFCD03788155 | |
Melting Point: | Boiling Point: | ||
Density: | 1.04g/mL | Storage Condition: | room temperature, dry |
Product Description:
This chemical is widely used in organic synthesis as a protecting group for amines, particularly in peptide synthesis. Its tert-butoxycarbonyl (Boc) group shields the amine functionality during reactions, preventing unwanted side reactions. After the desired chemical transformations are complete, the Boc group can be selectively removed under mild acidic conditions, restoring the free amine. This makes it highly valuable in the production of complex molecules, including pharmaceuticals and biologically active compounds. Additionally, its ethylenedioxy diethylamine structure provides stability and compatibility with various reaction conditions, making it a versatile tool in synthetic chemistry.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless to Yellow Viscous Liquid |
PROTON NMR SPECTRUM | Conforms to Structure |
PURITYHPLC | 94.5 100% |
REFRACTIVE INDEX N20D | 1.45-1.47 |
SPECIFIC GRAVITY 2020C | 1.04-1.05 |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿350.00 |
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1.000 | 10-20 days | ฿1,080.00 |
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5.000 | 10-20 days | ฿4,160.00 |
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N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine
This chemical is widely used in organic synthesis as a protecting group for amines, particularly in peptide synthesis. Its tert-butoxycarbonyl (Boc) group shields the amine functionality during reactions, preventing unwanted side reactions. After the desired chemical transformations are complete, the Boc group can be selectively removed under mild acidic conditions, restoring the free amine. This makes it highly valuable in the production of complex molecules, including pharmaceuticals and biologically active compounds. Additionally, its ethylenedioxy diethylamine structure provides stability and compatibility with various reaction conditions, making it a versatile tool in synthetic chemistry.
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