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
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
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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