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CAS 500770-75-2

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Boc-L-3-Amino-3-(2-bromophenyl)-propionic acid

Description:
Boc-L-3-Amino-3-(2-bromophenyl)-propionic acid is a synthetic amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group, which enhances its stability and solubility in organic solvents. The compound features a 3-amino group attached to a propionic acid backbone, along with a 2-bromophenyl substituent that contributes to its unique chemical properties. This structure allows for potential applications in peptide synthesis and medicinal chemistry, particularly in the development of bioactive compounds. The bromine atom in the phenyl ring can participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a versatile building block in organic synthesis. Additionally, the presence of the carboxylic acid group provides acidic properties, while the amino group can engage in hydrogen bonding and other interactions, influencing the compound's reactivity and solubility. Overall, Boc-L-3-Amino-3-(2-bromophenyl)-propionic acid is a valuable compound in the field of organic and medicinal chemistry.
Formula:C14H18BrNO4
InChI:InChI=1/C14H18BrNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-6-4-5-7-10(9)15/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)
SMILES:CC(C)(C)OC(=NC(CC(=O)O)c1ccccc1Br)O
Synonyms:
  • 3-(2-Bromophenyl)-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)propanoic acid
  • Benzenepropanoic Acid, 2-Bromo-Β-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-
  • 3-(2-Bromophenyl)-3-[(Tert-Butoxycarbonyl)Amino]Propanoic Acid
  • Boc-(S)-3-Amino-3-(2-bromophenyl)-propionic acid
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