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CAS 137255-86-8

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(S)-METHYL N-TERT-BUTOXYCARBONYL-3-(4-BIPHENYLYL)-2-AMINOPROPIONATE

Description:
(S)-Methyl N-tert-butoxycarbonyl-3-(4-biphenylyl)-2-aminopropionate, with CAS number 137255-86-8, is a chiral compound that belongs to the class of amino acid derivatives. It features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in peptide synthesis to protect the amino group during chemical reactions. The presence of the biphenyl moiety contributes to its hydrophobic characteristics, potentially influencing its solubility and interaction with biological systems. This compound is typically utilized in the synthesis of pharmaceuticals and biologically active molecules, particularly in the development of peptide-based drugs. Its stereochemistry, indicated by the (S) configuration, is crucial for its biological activity, as the spatial arrangement of atoms can significantly affect how the molecule interacts with biological targets. Overall, this compound exemplifies the complexity and specificity required in the design of bioactive molecules in medicinal chemistry.
Formula:C21H25NO4
InChI:InChI=1/C21H25NO4/c1-21(2,3)26-20(24)22-18(19(23)25-4)14-15-10-12-17(13-11-15)16-8-6-5-7-9-16/h5-13,18H,14H2,1-4H3,(H,22,24)/t18-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccc(cc1)c1ccccc1)C(=O)OC)O
Synonyms:
  • Rarechem Ah Ck 0053
  • Methyl-2-(S)-N-Boc-Amino-2-Biphenyl Propionate
  • (S)-Methyl N-tert-butoxycarbonyl-3-(4-biphenylyl)-2-aminopropionate 98%
  • (S)-N-Tert-Butoxycarbonyl-3-(4-Biphenylyl)-2-Aminopropanoic Acid Methyl Ester
  • Methyl 3-Biphenyl-4-Yl-2-[(Tert-Butoxycarbonyl)Amino]Propanoate (Non-Preferred Name)
  • methyl (2S)-3-(biphenyl-4-yl)-2-[(tert-butoxycarbonyl)amino]propanoate (non-preferred name)
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