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CAS 284493-53-4

:

3-N-BOC-Amino-3-(3-methoxyphenyl)propionicacid

Description:
3-N-BOC-Amino-3-(3-methoxyphenyl)propionic acid, identified by its CAS number 284493-53-4, is an amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amino group and a methoxyphenyl substituent on the propionic acid backbone. This compound typically exhibits properties associated with amino acids, such as the ability to form hydrogen bonds and participate in various chemical reactions, including peptide bond formation. The BOC group serves as a protective moiety, making the amino group less reactive during synthetic procedures, which is advantageous in peptide synthesis. The methoxyphenyl group contributes to the compound's hydrophobic character and can influence its solubility and interaction with biological systems. Overall, this compound is of interest in pharmaceutical and biochemical research, particularly in the development of peptide-based therapeutics and as a building block in organic synthesis. Its stability, reactivity, and functional group characteristics make it a valuable compound in medicinal chemistry.
Formula:C15H20NO5
InChI:InChI=1/C15H21NO5/c1-15(2,3)21-14(19)16-12(9-13(17)18)10-6-5-7-11(8-10)20-4/h5-8,12H,9H2,1-4H3,(H,16,19)(H,17,18)/p-1/t12-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](CC(=O)[O-])c1cccc(c1)OC)O
Synonyms:
  • 3-(Boc-amino)-3-(3-methoxyphenyl)propionic acid
  • 3-(tert-Butoxycarbonylamino)-3-(3-methoxyphenyl)propionic acid
  • 3-[(Tert-Butoxycarbonyl)Amino]-3-(3-Methoxyphenyl)Propanoic Acid
  • (3S)-3-[(tert-butoxycarbonyl)amino]-3-(3-methoxyphenyl)propanoate
  • (3R)-3-[(tert-butoxycarbonyl)amino]-3-(3-methoxyphenyl)propanoate
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