(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-bromophenyl)propanoic acid

98%

  • Product Code: 104186
  CAS:    220497-81-4
Molecular Weight: 466.32 g./mol Molecular Formula: C₂₄H₂₀BrNO₄
EC Number: MDL Number: MFCD01311771
Melting Point: Boiling Point: 660.8°C at 760 mmHg
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during the synthesis process. The bromophenyl moiety can be utilized for further functionalization or as a handle for cross-coupling reactions in organic synthesis. Its application is significant in the development of pharmaceuticals and bioactive peptides, where precise control over amino acid sequences is crucial. Additionally, the presence of the bromine atom makes it a valuable intermediate in the synthesis of complex organic molecules, particularly in medicinal chemistry for the design of drug candidates.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿1,260.00
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1.000 10-20 days ฿3,420.00
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5.000 10-20 days ฿14,814.00
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-bromophenyl)propanoic acid
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during the synthesis process. The bromophenyl moiety can be utilized for further functionalization or as a handle for cross-coupling reactions in organic synthesis. Its application is significant in the development of pharmaceuticals and bioactive peptides, where precise control over amino acid sequences is crucial. Additionally, the presence of the bromine atom makes it a valuable intermediate in the synthesis of complex organic molecules, particularly in medicinal chemistry for the design of drug candidates.
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