Description

Naphthalenylthioethyl acrylate (CAS No. 897049-32-0) is a specialized acrylate ester featuring a naphthalenylthioethyl functional group, with the molecular formula C₁₅H₁₄O₂S. This high-purity compound is designed for advanced research and industrial applications, particularly in polymer chemistry and material science. Its IUPAC name, 2-naphthalen-2-ylsulfanylethyl prop-2-enoate, reflects its unique structure, combining a naphthalene moiety with a reactive acrylate group through a thioether linkage. This configuration enables versatile reactivity, making it valuable for synthesizing functionalized polymers, photoresists, and specialty coatings. The product is rigorously tested for quality, ensuring optimal performance in demanding experimental conditions. Store in a cool, dry place under inert atmosphere to maintain stability.

Properties

• CAS Number: 897049-32-0
• Complexity: 290
• IUPAC Name: 2-(2-naphthylsulfanyl)ethyl prop-2-enoate
• InChI: InChI=1S/C15H14O2S/c1-2-15(16)17-9-10-18-14-8-7-12-5-3-4-6-13(12)11-14/h2-8,11H,1,9-10H2
• InChI Key: TVQDRZGNLJFEQK-UHFFFAOYSA-N
• Exact Mass: 258.07145086
• Molecular Formula: C15H14O2S
• Molecular Weight: 258.3
• SMILES: C=CC(=O)OCCSC1=CC2=CC=CC=C2C=C1
• Topological: 51.6
• Monoisotopic Mass: 258.07145086
• Synonyms: 897049-32-0, NAPHTHALENYLTHIOETHYL ACRYLATE, 2-Propenoic acid 2-(2-naphthalenylthio)ethyl ester, 2-naphthalen-2-ylsulfanylethyl prop-2-enoate, SCHEMBL1491949, 2-(Naphthalen-2-ylthio)ethyl acrylate, DB-078470

Application

Naphthalenylthioethyl acrylate is primarily used as a monomer in the synthesis of advanced polymeric materials, where its naphthalene group enhances thermal stability and optical properties. It is also employed in photolithography and resist formulations due to its UV-reactive acrylate moiety. Researchers utilize this compound to develop functionalized surfaces and coatings with tailored adhesion and chemical resistance.

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