Description

6-(Dimethylamino)-2-naphthaldehyde (CAS No. 173471-71-1) is a high-purity organic compound with the molecular formula C₁₃H₁₃NO, widely utilized in fluorescence studies and as a key intermediate in organic synthesis. This naphthalene derivative features a dimethylamino electron-donating group and an aldehyde functionality, making it an excellent fluorophore and a versatile building block for the development of fluorescent probes, sensors, and advanced materials. Its strong solvatochromic properties allow for applications in polarity-sensitive studies. Suitable for researchers in photochemistry, materials science, and bioimaging, this product is rigorously tested for purity and consistency, ensuring reliable performance in sensitive experiments. Available in various quantities to meet both research and industrial-scale demands.

Properties

• CAS Number: 173471-71-1
• Complexity: 227
• IUPAC Name: 6-(dimethylamino)naphthalene-2-carbaldehyde
• InChI: InChI=1S/C13H13NO/c1-14(2)13-6-5-11-7-10(9-15)3-4-12(11)8-13/h3-9H,1-2H3
• InChI Key: IVFSOOIWIYPDLX-UHFFFAOYSA-N
• Exact Mass: 199.099714038
• Molecular Formula: C13H13NO
• Molecular Weight: 199.25
• SMILES: CN(C)C1=CC2=C(C=C1)C=C(C=C2)C=O
• Topological: 20.3
• Monoisotopic Mass: 199.099714038
• Synonyms: 6-(Dimethylamino)-2-naphthaldehyde, 173471-71-1, 6-Dimethylamino-2-naphthaldehyde, 6-(dimethylamino)naphthalene-2-carbaldehyde, 2-Naphthalenecarboxaldehyde, 6-(dimethylamino)-, MFCD07776686, 6-(Dimethylamino)-2-naphthalenecarboxaldehyde, SCHEMBL1395192, SCHEMBL3490748, DTXSID20649016, IVFSOOIWIYPDLX-UHFFFAOYSA-N, AKOS006230135, GS-3714, 6-(N,N-dimethylamino)-2-naphthaldehyde, SY107624, DB-359206, CS-0018968

Application

6-(Dimethylamino)-2-naphthaldehyde is primarily used as a fluorescent probe due to its solvatochromic behavior, enabling the study of microenvironment polarity in chemical and biological systems. It serves as a precursor for synthesizing naphthalimide derivatives, which are applied in optoelectronic materials and sensors. The compound is also employed in the development of pH-sensitive dyes and as a labeling reagent for biomolecules. Its high fluorescence quantum yield makes it valuable in photophysical research and imaging applications.

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