3-((tert-Butoxycarbonyl)(methoxy)amino)propanoic acid
95%
- Product Code: 67456
CAS:
172299-81-9
| Molecular Weight: | 219.24 g./mol | Molecular Formula: | C₉H₁₇NO₅ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 327.8°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a protective group for amines during complex chemical reactions, ensuring that specific functional groups remain unaffected while other parts of the molecule undergo modification. Its tert-butoxycarbonyl (Boc) group is especially valuable in peptide synthesis, as it can be easily removed under mild acidic conditions without disrupting the peptide backbone. Additionally, the methoxy group provides further stability and selectivity in synthetic processes. This compound is often employed in the pharmaceutical industry for the development of drug candidates and in academic research for studying biochemical pathways and molecular interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,539.00 |
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| 1.000 | 10-20 days | ฿3,708.00 |
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3-((tert-Butoxycarbonyl)(methoxy)amino)propanoic acid
This chemical is primarily utilized in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a protective group for amines during complex chemical reactions, ensuring that specific functional groups remain unaffected while other parts of the molecule undergo modification. Its tert-butoxycarbonyl (Boc) group is especially valuable in peptide synthesis, as it can be easily removed under mild acidic conditions without disrupting the peptide backbone. Additionally, the methoxy group provides further stability and selectivity in synthetic processes. This compound is often employed in the pharmaceutical industry for the development of drug candidates and in academic research for studying biochemical pathways and molecular interactions.
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