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CAS 181140-88-5

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(R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID

Description:
(R)-3-(tert-Butoxycarbonylamino)-2-phenylpropanoic acid, with the CAS number 181140-88-5, is an amino acid derivative characterized by its chiral center, which imparts specific stereochemical properties. This compound features a tert-butoxycarbonyl (Boc) protecting group on the amino group, enhancing its stability and solubility in organic solvents. The presence of the phenyl group contributes to its hydrophobic characteristics, while the carboxylic acid functional group provides acidic properties, allowing for potential interactions in biological systems. The compound is typically utilized in peptide synthesis and as an intermediate in organic synthesis due to its ability to form stable amide bonds. Its chirality is significant in pharmaceutical applications, as the (R)-enantiomer may exhibit different biological activities compared to its (S)-counterpart. Overall, this compound is of interest in medicinal chemistry and biochemistry for its potential applications in drug development and synthesis.
Formula:C14H19NO4
Synonyms:
  • (2R)-3-{[(tert-butoxy)carbonyl]amino}-2-phenylpropanoic acid
  • (R)-BOC-BETA2-PHENYLALANINE
  • (R)-3-tert-Butoxycarbonylamino-2-phenyl-propionic acid
  • Benzeneacetic acid, α-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]-, (αR)-
  • (R)-3-(Boc-aMino)-2-phenylpropionic acid
  • Boc-(R)-3-aMino-2-phenylpropanoic acid
  • (Tert-Butoxy)Carbonyl (R)-3-Amino-2-phenylpropanoic acid
  • (R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID
  • BMOC-(R)-3-AMINO-2-PHENYLPROPANOICACID
  • Benzeneacetic acid ,a-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]-,(R)-(9Cl)
  • (2R)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-2-phenylpropanoic acid
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