(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(3-chlorophenyl)butanoic acid

98%

  • Product Code: 64677
  CAS:    331763-57-6
Molecular Weight: 435.900 g./mol Molecular Formula: C₂₅H₂₂ClNO₄
EC Number: MDL Number: MFCD01860902
Melting Point: Boiling Point: 653.6±55.0 °C at 760 mmHg
Density: 1.3±0.1 g/cm3 Storage Condition: room temperature
Product Description: This chemical is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the synthesis process. The presence of the 3-chlorophenyl moiety adds specific structural characteristics, making it valuable for designing peptides with tailored properties, such as enhanced binding affinity or stability. Its application is particularly significant in the development of pharmaceuticals, where precise peptide sequences are required for drug discovery and therapeutic agents. Additionally, it is utilized in research settings to study peptide interactions and modifications, contributing to advancements in biochemistry and molecular biology.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,899.00
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0.250 10-20 days ฿3,447.00
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1.000 10-20 days ฿7,758.00
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(3-chlorophenyl)butanoic acid
This chemical is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the synthesis process. The presence of the 3-chlorophenyl moiety adds specific structural characteristics, making it valuable for designing peptides with tailored properties, such as enhanced binding affinity or stability. Its application is particularly significant in the development of pharmaceuticals, where precise peptide sequences are required for drug discovery and therapeutic agents. Additionally, it is utilized in research settings to study peptide interactions and modifications, contributing to advancements in biochemistry and molecular biology.
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