(S)-4-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid

98%

  • Product Code: 60732
  CAS:    270062-85-6
Molecular Weight: 358.23 g./mol Molecular Formula: C₁₅H₂₀BrNO₄
EC Number: MDL Number: MFCD01861015
Melting Point: Boiling Point: 491.9℃°C at 767 mmHg
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that target specific biological pathways. It serves as a key intermediate in the production of drugs that modulate neurotransmitter systems, potentially aiding in the treatment of neurological disorders such as depression, anxiety, or Parkinson's disease. Additionally, its structure, featuring a bromophenyl group and a protected amino acid moiety, makes it valuable in peptide chemistry for constructing complex peptide-based therapeutics. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling precise control during multi-step synthetic processes. This compound is also utilized in research settings for studying enzyme interactions and designing inhibitors for specific enzymes involved in disease mechanisms.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿2,133.00
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0.250 10-20 days ฿4,365.00
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1.000 10-20 days ฿10,908.00
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(S)-4-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid
This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that target specific biological pathways. It serves as a key intermediate in the production of drugs that modulate neurotransmitter systems, potentially aiding in the treatment of neurological disorders such as depression, anxiety, or Parkinson's disease. Additionally, its structure, featuring a bromophenyl group and a protected amino acid moiety, makes it valuable in peptide chemistry for constructing complex peptide-based therapeutics. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling precise control during multi-step synthetic processes. This compound is also utilized in research settings for studying enzyme interactions and designing inhibitors for specific enzymes involved in disease mechanisms.
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