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Atomfair Methyl 2-amino-4-((tert-butoxycarbonyl)amino)benzoate C13H18N2O4

Description Methyl 2-amino-4-((tert-butoxycarbonyl)amino)benzoate (CAS No. 849792-91-2) is a high-purity chemical compound with the molecular formula C13H18N2O4. This specialized intermediate features a benzoate ester core functionalized with both an amino group and a tert-butoxycarbonyl (Boc)-protected amino group at the 2- and 4-positions, respectively. Its IUPAC name is methyl 2-amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoate . The Boc group provides orthogonal protection for amines in multi-step synthetic routes, making this compound invaluable in peptide synthesis , medicinal chemistry , and pharmaceutical research . Supplied as a crystalline solid with ??95% purity (HPLC), it is rigorously tested by GC-MS,1H/13C NMR, and elemental analysis to ensure batch-to-batch consistency. Store…

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Description

Description

Methyl 2-amino-4-((tert-butoxycarbonyl)amino)benzoate (CAS No. 849792-91-2) is a high-purity chemical compound with the molecular formula C13H18N2O4. This specialized intermediate features a benzoate ester core functionalized with both an amino group and a tert-butoxycarbonyl (Boc)-protected amino group at the 2- and 4-positions, respectively. Its IUPAC name is methyl 2-amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoate. The Boc group provides orthogonal protection for amines in multi-step synthetic routes, making this compound invaluable in peptide synthesis, medicinal chemistry, and pharmaceutical research. Supplied as a crystalline solid with ??95% purity (HPLC), it is rigorously tested by GC-MS, 1H/13C NMR, and elemental analysis to ensure batch-to-batch consistency. Store under inert atmosphere at 2-8??C to maintain stability.

  • CAS No: 849792-91-2
  • Molecular Formula: C13H18N2O4
  • Molecular Weight: 266.29
  • Exact Mass: 266.12665706
  • Monoisotopic Mass: 266.12665706
  • IUPAC Name: methyl 2-amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoate
  • SMILES: CC(C)(C)OC(=O)NC1=CC(=C(C=C1)C(=O)OC)N
  • Synonyms: 849792-91-2, Methyl 2-amino-4-((tert-butoxycarbonyl)amino)benzoate, methyl 2-amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoate, Benzoic acid, 2-amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester, Methyl 2-amino-4-[(tert-butoxycarbonyl)amino]benzoate

Application

This Boc-protected aminobenzoate derivative serves as a key building block in the synthesis of non-natural amino acids and peptidomimetics. It is particularly useful in constructing fluorescence probes due to its aromatic amine functionality. Researchers employ it in protease inhibitor development where the ester moiety allows further functionalization. The compound’s orthogonal protection scheme enables selective deprotection in complex multi-step organic syntheses.

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