5-(4-(((((9H-Fluoren-9-yl methoxy)carbonyl)amino)methyl))-3,5-dimethoxy phenoxy]pentanoic acid

97%

  • Product Code: 124349
  Alias:    5-[4-[[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3,5-dimethoxyphenoxy]pentanoic acid
  CAS:    115109-65-4
Molecular Weight: 505.56 g./mol Molecular Formula: C₂₉H₃₁NO₇
EC Number: MDL Number: MFCD00236731
Melting Point: Boiling Point: 733.0℃ at 760 mmHg (Predicted)
Density: 1.2g/cm3 Storage Condition: 2-8℃
Product Description: This chemical is primarily used in the field of peptide synthesis, where it serves as a key building block. It is particularly valuable for introducing specific functional groups into peptide chains during solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for amines, ensuring selective deprotection and controlled assembly of peptide sequences. The compound’s structure, featuring a pentanoic acid moiety, allows for efficient coupling reactions, while the dimethoxy phenoxy group enhances stability and solubility in organic solvents. Its application is critical in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days £162.84
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5-(4-(((((9H-Fluoren-9-yl methoxy)carbonyl)amino)methyl))-3,5-dimethoxy phenoxy]pentanoic acid
This chemical is primarily used in the field of peptide synthesis, where it serves as a key building block. It is particularly valuable for introducing specific functional groups into peptide chains during solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for amines, ensuring selective deprotection and controlled assembly of peptide sequences. The compound’s structure, featuring a pentanoic acid moiety, allows for efficient coupling reactions, while the dimethoxy phenoxy group enhances stability and solubility in organic solvents. Its application is critical in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies.
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