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CAS 269396-71-6

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Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid

Description:
Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid is a chemical compound characterized by its structure, which includes a butyric acid backbone with an amino group and a Boc (tert-butyloxycarbonyl) protecting group. The presence of the 4-iodo-phenyl substituent introduces significant steric and electronic effects, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals. The Boc group serves as a protective moiety for the amino group, facilitating various chemical reactions without the risk of amine reactivity. This compound is typically used in peptide synthesis and medicinal chemistry, where the chirality of the (R) configuration can influence biological activity. Its solubility and stability are influenced by the presence of the iodo substituent and the Boc group, which can affect its interaction with biological targets. As with many amino acids and their derivatives, it is essential to handle this compound with care, considering potential hazards associated with iodine-containing compounds.
Formula:C15H20INO4
InChI:InChI=1/C15H20INO4/c1-15(2,3)21-14(20)17-12(9-13(18)19)8-10-4-6-11(16)7-5-10/h4-7,12H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t12-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](Cc1ccc(cc1)I)CC(=O)O)O
Synonyms:
  • Boc-D-3-Amino-4-(4-iodophenyl)-butyric acid
  • (3R)-3-[(tert-butoxycarbonyl)amino]-4-(4-iodophenyl)butanoic acid
  • Boc-D-β-HoPhe(4-I)-OH
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