2-((tert-Butoxycarbonyl)amino)-3-(pyridin-4-yl)propanoic acid
97%
- Product Code: 58251
CAS:
33814-94-7
Molecular Weight: | 266.29 g./mol | Molecular Formula: | C₁₃H₁₈N₂O₄ |
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EC Number: | MDL Number: | MFCD06656857 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, particularly peptides and small molecule drugs. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions at other sites. Additionally, the pyridine moiety in its structure makes it valuable for designing molecules with specific binding properties, often targeting enzymes or receptors. Its applications extend to the development of potential therapeutic agents, including those for neurological disorders, due to its ability to mimic certain natural amino acids and interact with biological systems.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,314.00 |
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1.000 | 10-20 days | ฿3,528.00 |
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5.000 | 10-20 days | ฿12,249.00 |
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2-((tert-Butoxycarbonyl)amino)-3-(pyridin-4-yl)propanoic acid
This chemical is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, particularly peptides and small molecule drugs. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions at other sites. Additionally, the pyridine moiety in its structure makes it valuable for designing molecules with specific binding properties, often targeting enzymes or receptors. Its applications extend to the development of potential therapeutic agents, including those for neurological disorders, due to its ability to mimic certain natural amino acids and interact with biological systems.
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