(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-2-methyl-4-oxobutanoic acid

≥95%

  • Product Code: 38049
  CAS:    1072845-47-6
Molecular Weight: 425.47 g./mol Molecular Formula: C₂₄H₂₇NO₆
EC Number: MDL Number: MFCD12031692
Melting Point: Boiling Point: 623.0±55.0°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides, ensuring specific amino acids are incorporated correctly during solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amine functionality, preventing unwanted reactions during the synthesis process. The tert-butoxy group protects the carboxylic acid moiety, allowing selective deprotection and activation when needed. This compound is particularly valuable in the production of peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide structure is critical. Its application is essential in synthesizing peptides with high purity and yield, making it a key reagent in modern peptide chemistry.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $748.57
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0.250 10-20 days $1,497.14
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-2-methyl-4-oxobutanoic acid
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides, ensuring specific amino acids are incorporated correctly during solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amine functionality, preventing unwanted reactions during the synthesis process. The tert-butoxy group protects the carboxylic acid moiety, allowing selective deprotection and activation when needed. This compound is particularly valuable in the production of peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide structure is critical. Its application is essential in synthesizing peptides with high purity and yield, making it a key reagent in modern peptide chemistry.
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