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CAS 77171-41-6

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N-Boc-(2R,3R)-2-Hydroxy-3-Amino-4-Phenylbutanoic Acid

Description:
N-Boc-(2R,3R)-2-Hydroxy-3-Amino-4-Phenylbutanoic Acid, with the CAS number 77171-41-6, is a chemical compound that belongs to the class of amino acids and is characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group. This compound features a chiral center, indicated by the (2R,3R) configuration, which contributes to its stereochemical properties. The molecule contains a hydroxyl group (-OH) and an amino group (-NH2), making it a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and peptides. The phenyl group attached to the butanoic acid backbone enhances its hydrophobic characteristics, influencing its solubility and interaction with biological systems. N-Boc protection is commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. Overall, this compound is significant in medicinal chemistry and biochemistry due to its structural features and functional groups that facilitate various chemical reactions and applications.
Formula:C15H21NO5
InChI:InChI=1/C15H21NO5/c1-15(2,3)21-14(20)16-11(12(17)13(18)19)9-10-7-5-4-6-8-10/h4-8,11-12,17H,9H2,1-3H3,(H,16,20)(H,18,19)/t11-,12-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccccc1)[C@@H](C(=O)O)O)O
Synonyms:
  • (2S,3S)-3-[(tert-butoxycarbonyl)amino]-2-hydroxy-4-phenylbutanoic acid
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