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CAS 132691-45-3

:

3-(4-((Tert-butoxycarbonylamino)methyl)phenyl)propanoic acid

Description:
3-(4-((Tert-butoxycarbonylamino)methyl)phenyl)propanoic acid, with CAS number 132691-45-3, is an organic compound characterized by its structure, which includes a propanoic acid moiety and a phenyl group substituted with a tert-butoxycarbonyl (Boc) protected amino group. This compound typically appears as a white to off-white solid and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the presence of the phenyl and tert-butoxycarbonyl groups. The Boc group serves as a protective group for the amino functionality, making it useful in peptide synthesis and other organic reactions where selective deprotection is required. The presence of the carboxylic acid functional group indicates that it can participate in acid-base reactions and may act as a weak acid. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research and development. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application.
Formula:C15H21NO4
InChI:InChI=1S/C15H21NO4/c1-15(2,3)20-14(19)16-10-12-6-4-11(5-7-12)8-9-13(17)18/h4-7H,8-10H2,1-3H3,(H,16,19)(H,17,18)
InChI key:InChIKey=VCUMJMFHSOBLMG-UHFFFAOYSA-N
SMILES:C(NC(OC(C)(C)C)=O)C1=CC=C(CCC(O)=O)C=C1
Synonyms:
  • Benzenepropanoic acid, 4-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]-
  • 3-[4-[[(tert-Butoxycarbonyl)amino]methyl]phenyl]propanoic acid
  • 4-[[[(1,1-Dimethylethoxy)carbonyl]amino]methyl]benzenepropanoic acid
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