(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((diphenyl(p-tolyl)methyl)amino)butanoic acid

95%

  • Product Code: 104195
  CAS:    1217809-38-5
Molecular Weight: 596.71 g./mol Molecular Formula: C₃₉H₃₆N₂O₄
EC Number: MDL Number: MFCD02094100
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily utilized in the field of peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for the introduction of specific amino acids into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino function, ensuring selective reactions during the synthesis process. The diphenyl(p-tolyl)methyl (Trt) group protects the side chain of the amino acid, preventing unwanted side reactions. Its application is crucial in the production of complex peptides and proteins, which are widely used in pharmaceutical research, drug development, and biochemical studies. The compound’s stability and compatibility with SPPS protocols make it a valuable tool for synthesizing peptides with high precision and efficiency.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿810.00
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0.250 10-20 days ฿1,368.00
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-
1.000 10-20 days ฿3,681.00
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((diphenyl(p-tolyl)methyl)amino)butanoic acid
This chemical is primarily utilized in the field of peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for the introduction of specific amino acids into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino function, ensuring selective reactions during the synthesis process. The diphenyl(p-tolyl)methyl (Trt) group protects the side chain of the amino acid, preventing unwanted side reactions. Its application is crucial in the production of complex peptides and proteins, which are widely used in pharmaceutical research, drug development, and biochemical studies. The compound’s stability and compatibility with SPPS protocols make it a valuable tool for synthesizing peptides with high precision and efficiency.
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