(S)-3-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoyl)-2,2-dimethyloxazolidine-4-carboxylic acid

98%

  • Product Code: 38374
  CAS:    878797-09-2
Molecular Weight: 586.6700 g./mol Molecular Formula: C₃₄H₃₈N₂O₇
EC Number: MDL Number: MFCD11974986
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This compound is primarily utilized in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group safeguards the amino functionality during the synthesis process, preventing unwanted side reactions. The tert-butoxy group on the phenyl ring provides additional stability under acidic conditions, making it suitable for stepwise peptide assembly. The oxazolidine moiety acts as a chiral auxiliary, ensuring the stereochemical integrity of the synthesized peptides. This chemical is particularly valuable in solid-phase peptide synthesis (SPPS), where high purity and specificity are critical. Its application is essential in producing peptides for pharmaceutical research, drug development, and biochemical studies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days £80.81
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(S)-3-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoyl)-2,2-dimethyloxazolidine-4-carboxylic acid
This compound is primarily utilized in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group safeguards the amino functionality during the synthesis process, preventing unwanted side reactions. The tert-butoxy group on the phenyl ring provides additional stability under acidic conditions, making it suitable for stepwise peptide assembly. The oxazolidine moiety acts as a chiral auxiliary, ensuring the stereochemical integrity of the synthesized peptides. This chemical is particularly valuable in solid-phase peptide synthesis (SPPS), where high purity and specificity are critical. Its application is essential in producing peptides for pharmaceutical research, drug development, and biochemical studies.
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