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CAS 133887-83-9

:

3,5-BIS-BOC-AMINOBENZOIC ACID

Description:
3,5-Bis-Boc-aminobenzoic acid is a chemical compound characterized by the presence of two tert-butyloxycarbonyl (Boc) protecting groups attached to the amino groups of a benzoic acid derivative. This compound features a benzene ring with carboxylic acid functionality, which contributes to its acidic properties. The Boc groups serve to protect the amine functionalities during synthetic processes, making the compound useful in peptide synthesis and other organic reactions. The presence of the carboxylic acid group allows for potential interactions such as hydrogen bonding and can influence solubility in various solvents. Typically, compounds like this are utilized in medicinal chemistry and biochemistry for the development of pharmaceuticals or as intermediates in the synthesis of more complex molecules. Its CAS number, 133887-83-9, allows for easy identification and retrieval of information regarding its properties, safety data, and applications in chemical databases. Overall, 3,5-bis-Boc-aminobenzoic acid is a versatile compound in organic synthesis with specific protective and functional characteristics.
Formula:C17H24N2O6
InChI:InChI=1/C17H24N2O6/c1-16(2,3)24-14(22)18-11-7-10(13(20)21)8-12(9-11)19-15(23)25-17(4,5)6/h7-9H,1-6H3,(H,18,22)(H,19,23)(H,20,21)
SMILES:CC(C)(C)OC(=Nc1cc(cc(c1)N=C(O)OC(C)(C)C)C(=O)O)O
Synonyms:
  • Bis-Boc-3,5-Diaminobenzoic Acid
  • Bis-Tert-Butyloxycarbonyl-3,5-Diaminobenzoic Acid
  • Boc2-3,5-Daba-Oh
  • Di-Boc-3,5-Diaminobenzoic Acid
  • Bis-T-Butyloxycarbonyl-3,5-Diaminobenzoic Acid
  • 3,5-Bis[(Tert-Butoxycarbonyl)Amino]Benzoic Acid
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