Atomfair Bis(1-methyl-2-oxopropyl) sulfide C8H14O2S

Description Bis(1-methyl-2-oxopropyl) sulfide (CAS No. 113334-17-1) is a high-purity organic compound with the molecular formula C8H14O2S and IUPAC name 3-(3-oxobutan-2-ylsulfanyl)butan-2-one . This specialized chemical is ideal for research and industrial applications requiring precise sulfur-containing ketone derivatives. Its unique structure features two acetyl-substituted methyl groups bridged by a sulfur atom, making it valuable for synthetic organic chemistry, coordination studies, and material science applications. Available in rigorously controlled purity grades, this compound is supplied with comprehensive analytical documentation including1H NMR,13C NMR, and GC-MS data to ensure reproducibility in your research. Proper storage under inert atmosphere at 2-8??C is recommended to maintain stability.

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Description

Description

Bis(1-methyl-2-oxopropyl) sulfide (CAS No. 113334-17-1) is a high-purity organic compound with the molecular formula C8H14O2S and IUPAC name 3-(3-oxobutan-2-ylsulfanyl)butan-2-one. This specialized chemical is ideal for research and industrial applications requiring precise sulfur-containing ketone derivatives. Its unique structure features two acetyl-substituted methyl groups bridged by a sulfur atom, making it valuable for synthetic organic chemistry, coordination studies, and material science applications. Available in rigorously controlled purity grades, this compound is supplied with comprehensive analytical documentation including 1H NMR, 13C NMR, and GC-MS data to ensure reproducibility in your research. Proper storage under inert atmosphere at 2-8??C is recommended to maintain stability.

  • CAS No: 113334-17-1
  • Molecular Formula: C8H14O2S
  • Molecular Weight: 174.26
  • Exact Mass: 174.07145086
  • Monoisotopic Mass: 174.07145086
  • IUPAC Name: 3-(3-oxobutan-2-ylsulfanyl)butan-2-one
  • SMILES: CC(C(=O)C)SC(C)C(=O)C
  • Synonyms: bis(1-methyl-2-oxopropyl) sulfide, SCHEMBL6130000, YGVGCMGLHWUOCP-UHFFFAOYSA-N

Application

Bis(1-methyl-2-oxopropyl) sulfide serves as a versatile building block in organic synthesis, particularly for developing sulfur-containing heterocycles and metal coordination complexes. Researchers utilize this compound in studies of nucleophilic substitution reactions at sulfur centers and as a precursor for functionalized thioether derivatives. Its bifunctional carbonyl groups enable participation in various condensation and addition reactions, making it valuable for pharmaceutical intermediate synthesis.

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