Description

4-amino-N-(tert-butyl)benzamide (CAS No. 93483-71-7) is a high-purity organic compound with the molecular formula C₁₁H₁₆N₂O, widely utilized in pharmaceutical and chemical research. This white to off-white crystalline solid is characterized by its tert-butyl amide functional group and aromatic amine moiety, making it a valuable intermediate in synthetic chemistry. With a molecular weight of 192.26 g/mol, it offers excellent solubility in common organic solvents such as DMSO, methanol, and dichloromethane. Our product is rigorously tested for purity (≥98% by HPLC) and is supplied in sealed, light-resistant packaging to ensure stability. Ideal for medicinal chemistry, peptidomimetics, and drug discovery applications, this compound is a must-have for researchers seeking reliable building blocks for complex organic synthesis.

Properties

• CAS Number: 93483-71-7
• Complexity: 200
• IUPAC Name: 4-amino-N-tert-butyl-benzamide
• InChI: InChI=1S/C11H16N2O/c1-11(2,3)13-10(14)8-4-6-9(12)7-5-8/h4-7H,12H2,1-3H3,(H,13,14)
• InChI Key: IBSCJDKXUQIEPQ-UHFFFAOYSA-N
• Exact Mass: 192.126263138
• Molecular Formula: C11H16N2O
• Molecular Weight: 192.26
• SMILES: CC(C)(C)NC(=O)C1=CC=C(C=C1)N
• Topological: 55.1
• Monoisotopic Mass: 192.126263138
• Synonyms: 4-amino-N-(tert-butyl)benzamide, 4-amino-N-tert-butylbenzamide, 93483-71-7, (4-aminophenyl)-N-(tert-butyl)carboxamide, 4-amino-N-tert-butyl-benzamide, MFCD00461428, N-t-Butyl-4-aminobenzamide, SCHEMBL854187, SCHEMBL1176575, DTXSID90399612, CHEBI:191028, IBSCJDKXUQIEPQ-UHFFFAOYSA-N, 4-amino-n-(tert-butyl) benzamide, TDA48371, BBL002124, SBB080096, STK520560, AKOS000131855, DA-40384, VS-01022, Benzamide, 4-amino-N-(1,1-dimethylethyl)-, CS-0244695, ST45050728, EN300-28909, G19116, Z235362715

Application

4-amino-N-(tert-butyl)benzamide serves as a versatile intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and receptor modulators. Its tert-butyl amide group enhances steric hindrance, making it useful for studying structure-activity relationships (SAR) in drug design. Researchers also employ this compound in peptide coupling reactions and as a precursor for novel heterocyclic frameworks. Its stability and reactivity render it suitable for high-throughput screening and combinatorial chemistry applications.

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