Description
Sodium 4-(2-(thiophen-3-yl)ethoxy)butane-1-sulfonate (CAS No. 701917-11-5) is a high-purity sulfonate compound with the molecular formula C10H15NaO4S2. This specialized chemical features a thiophene moiety linked via an ethoxybutyl chain to a sulfonate group, making it a valuable intermediate for organic synthesis and material science applications. Its IUPAC name is sodium;4-(2-thiophen-3-ylethoxy)butane-1-sulfonate. Ideal for researchers in pharmaceuticals, polymer chemistry, and electrochemistry, this compound is supplied with comprehensive analytical data including 1H NMR, 13C NMR, and HPLC purity verification. Store in a cool, dry place under inert conditions to ensure stability.
Properties
- CAS Number: 701917-11-5
- Complexity: 277
- IUPAC Name: sodium;4-[2-(3-thienyl)ethoxy]butane-1-sulfonate
- InChI: InChI=1S/C10H16O4S2.Na/c11-16(12,13)8-2-1-5-14-6-3-10-4-7-15-9-10;/h4,7,9H,1-3,5-6,8H2,(H,11,12,13);/q;+1/p-1
- InChI Key: RKLXQSIJSCLYEN-UHFFFAOYSA-M
- Exact Mass: 286.03094558
- Molecular Formula: C10H15NaO4S2
- Molecular Weight: 286.3
- SMILES: C1=CSC=C1CCOCCCCS(=O)(=O)[O-].[Na+]
- Topological: 103
- Monoisotopic Mass: 286.03094558
- Synonyms: 744198-90-1, Sodium 4-(2-(thiophen-3-yl)ethoxy)butane-1-sulfonate, SCHEMBL23092137, 701917-11-5, sodium 2-(3-thienyl)ethyloxybutylsulfonate
Application
Sodium 4-(2-(thiophen-3-yl)ethoxy)butane-1-sulfonate is primarily used as a functional monomer or surfactant in conductive polymer synthesis, particularly for polythiophene derivatives. Its sulfonate group enhances solubility in aqueous systems, facilitating electrochemical deposition processes. Researchers also employ it in organic electronics and battery electrolyte formulations due to its ionic conductivity and structural versatility.
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