3-[(tert-Butoxycarbonyl)amino]benzoic Acid TCI B6959

Chemical Identity

Other names: Boc-3-Abz-OH · Boc-3-aminobenzoic Acid
CAS No.: 111331-82-9
Formula: C12H15NO4
Molecular weight: 237.26 g/mol
Purity: >98.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-[(2-methylpropan-2-yl)oxycarbonylamino]benzoic acid
SMILES: CC(C)(C)OC(=O)NC1=CC=CC(=C1)C(=O)O
InChIKey: SAPAUOFSCLCQJB-UHFFFAOYSA-N
MDL: MDL00235884
PubChem: CID 854162

Rp 980.700,00

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Berat 5g 25g

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TCI B6959 is 3-[(tert-butoxycarbonyl)amino]benzoic acid, a Boc-protected aminobenzoic acid building block widely used in peptide and medicinal chemistry. Its free carboxylic acid is ready for standard amide coupling, while the Boc group keeps the aromatic amine masked until acidic deprotection. This orthogonality makes it convenient for stepwise assembly of linkers, scaffolds, and analogue libraries. AMI Scientific offers 5 g and 25 g pack sizes; keep the material dry, cool, and away from strong acids and heat.

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Kadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. Synthesis doi:10.1055/a-1526-7657
(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. Organic Syntheses doi:10.15227/orgsyn.089.0394
IHLE et al. (1996). ChemInform Abstract: Preparation of 4‐Alkyl‐2‐(N‐(tert‐butoxycarbonyl)amino)pyridines by Alkylation, Nucleophilic Addition, and Acylation of 2‐(N‐(tert‐ Butoxycarbonyl)amino)‐4‐picoline.. ChemInform doi:10.1002/chin.199646162

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.