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CAS 127106-71-2

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Boc-(S)-3-amino-4-(4-nitro-phenyl)-butyric acid

Description:
Boc-(S)-3-amino-4-(4-nitro-phenyl)-butyric acid is a chemical compound characterized by its structure, which includes a butyric acid backbone with an amino group and a nitrophenyl substituent. The "Boc" (tert-butyloxycarbonyl) group serves as a protecting group for the amino functionality, making it useful in peptide synthesis and other organic reactions. The presence of the nitro group on the phenyl ring contributes to the compound's electronic properties, potentially influencing its reactivity and interactions in biological systems. This compound is typically utilized in medicinal chemistry and research applications, particularly in the development of pharmaceuticals. Its stereochemistry, indicated by the (S) designation, suggests that it has specific spatial arrangements that can affect its biological activity and interactions with enzymes or receptors. As with many amino acids and their derivatives, it may exhibit properties such as solubility in polar solvents and the ability to form hydrogen bonds, which are critical for its function in biological contexts.
Formula:C15H20N2O6
InChI:InChI=1/C15H20N2O6/c1-15(2,3)23-14(20)16-11(9-13(18)19)8-10-4-6-12(7-5-10)17(21)22/h4-7,11H,8-9H2,1-3H3,(H,16,20)(H,18,19)/t11-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccc(cc1)N(=O)=O)CC(=O)O)O
Synonyms:
  • (3S)-3-[(tert-butoxycarbonyl)amino]-4-(4-nitrophenyl)butanoic acid
  • Boc-β-HoPhe(4-NO2)-OH
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