Description

Tert-butyl naphthalen-1-ylcarbamate (CAS No. 72594-62-8) is a high-purity organic compound with the molecular formula C₁₅H₁₇NO₂. This specialized carbamate derivative features a tert-butyl group and a naphthalen-1-yl moiety, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Its IUPAC name, tert-butyl N-naphthalen-1-ylcarbamate, reflects its precise structural configuration. The compound is supplied as a crystalline solid with ≥95% purity (HPLC), ensuring consistency for demanding applications. Suitable for use in peptide synthesis, protecting group strategies, and as a precursor for bioactive molecules, this product is rigorously tested for quality, including NMR and mass spectrometry verification. Store under inert conditions at 2-8°C to maintain stability.

Properties

• CAS Number: 72594-62-8
• Complexity: 295
• IUPAC Name: tert-butyl N-(1-naphthyl)carbamate
• InChI: InChI=1S/C15H17NO2/c1-15(2,3)18-14(17)16-13-10-6-8-11-7-4-5-9-12(11)13/h4-10H,1-3H3,(H,16,17)
• InChI Key: SCDGPDBWNRGGIX-UHFFFAOYSA-N
• Exact Mass: 243.125928785
• Molecular Formula: C15H17NO2
• Molecular Weight: 243.30
• SMILES: CC(C)(C)OC(=O)NC1=CC=CC2=CC=CC=C21
• Topological: 38.3
• Monoisotopic Mass: 243.125928785
• Synonyms: tert-butyl naphthalen-1-ylcarbamate, 72594-62-8, DTXSID60406842, DTXCID70357694, 1-(N-BOC-Amino)naphthalene, tert-butyl N-naphthalen-1-ylcarbamate, MFCD07127697, TERT-BUTYL N-(NAPHTHALEN-1-YL)CARBAMATE, tert-Butylnaphthalen-1-ylcarbamate, N-Boc-1-naphthalenamine, a-Naphthyl-tert.-butylurethan, SCHEMBL2396852, SCHEMBL27820227, STL256160, AKOS003477474, BS-18013, SY317239, DB-074591, CS-0154410, D82144, EN300-716422, Z1258794267

Application

Tert-butyl naphthalen-1-ylcarbamate serves as a versatile amine-protecting group reagent in peptide synthesis, particularly for sterically hindered substrates. It is employed in the development of naphthalene-based pharmaceuticals and agrochemicals due to its stability under acidic conditions. Researchers also utilize it as a building block for fluorescent probes and materials science applications, leveraging its aromatic backbone.

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