Description

Trimethyl-[3-(4-methylthiophen-3-yl)oxypropyl]azanium;bromide (CAS No. 851010-43-0) is a high-purity quaternary ammonium compound with the molecular formula C₁₁H₂₀BrNOS. This specialized chemical features a trimethylazanium group linked to a propyloxy-substituted 4-methylthiophene moiety, offering unique reactivity and structural properties. The compound is supplied as a bromide salt, ensuring excellent solubility in polar organic solvents and water. With a molecular weight of 294.25 g/mol, this material is ideal for advanced organic synthesis, catalysis research, and pharmaceutical intermediate development. Each batch is rigorously analyzed by HPLC, NMR, and mass spectrometry to guarantee ≥95% purity, meeting the stringent requirements of research and industrial applications. Proper storage at 2-8°C in a tightly sealed container is recommended to maintain stability.

Properties

• CAS Number: 851010-43-0
• Complexity: 167
• IUPAC Name: trimethyl-[3-[(4-methyl-3-thienyl)oxy]propyl]ammonium;bromide
• InChI: InChI=1S/C11H20NOS.BrH/c1-10-8-14-9-11(10)13-7-5-6-12(2,3)4;/h8-9H,5-7H2,1-4H3;1H/q+1;/p-1
• InChI Key: HDBOCKQQTJFHFJ-UHFFFAOYSA-M
• Exact Mass: 293.04490
• Molecular Formula: C11H20BrNOS
• Molecular Weight: 294.25
• SMILES: CC1=CSC=C1OCCC[N+](C)(C)C.[Br-]
• Topological: 37.5
• Monoisotopic Mass: 293.04490
• Synonyms: SCHEMBL28041109, 851010-43-0, N,N,N-Trimethyl-3-((4-methylthiophen-3-yl)oxy)propan-1-aminium bromide

Application

This quaternary ammonium compound serves as a versatile building block in organic synthesis, particularly for constructing sulfur-containing heterocycles. Researchers utilize it in phase-transfer catalysis due to its amphiphilic structure. The 4-methylthiophene moiety makes it valuable for developing conjugated polymers with optoelectronic properties. In pharmaceutical research, it acts as a precursor for bioactive molecules targeting neurological pathways.

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