594-43-4 | Ethyl methyl sulfone

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$11.00
5g	98%	in stock	$46.00	$33.00
25g	98%	in stock	$167.00	$117.00
100g	95%	in stock	$542.00	$380.00

Description

• Catalog Number: AB46122
• Chemical Name: Ethyl methyl sulfone
• CAS Number: 594-43-4
• Molecular Formula: C3H8O2S
• Molecular Weight: 108.1594
• MDL Number: MFCD00015543
• SMILES: CCS(=O)(=O)C

Computed Properties

• Complexity: 105
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

Ethyl Methyl Sulfone, also known as EMS, is a versatile compound utilized in various chemical synthesis processes. In the realm of organic chemistry, EMS serves as a valuable building block for the creation of new molecules and compounds. Its unique chemical structure and reactivity make it particularly useful as a reagent in reactions involving sulfones and other functional groups.Ethyl Methyl Sulfone can act as a sulfone transfer reagent, participating in sulfone exchange reactions to introduce the sulfone group into different organic molecules. This allows chemists to modify the properties of organic compounds for various applications, such as drug development, materials science, and agrochemicals. Additionally, EMS can undergo oxidation and reduction reactions, further expanding its utility in synthesis.Furthermore, Ethyl Methyl Sulfone can be involved in cross-coupling reactions, where it serves as a coupling partner to form carbon-carbon or carbon-heteroatom bonds. This aspect of its reactivity is particularly significant in the field of pharmaceutical chemistry, where the construction of complex molecular structures is essential for the development of new drugs.Overall, Ethyl Methyl Sulfone plays a crucial role in chemical synthesis by enabling the creation of diverse and complex organic molecules with specific functionalities. Its versatility and compatibility with a wide range of reaction conditions make it a valuable tool for organic chemists seeking to explore new avenues in molecular design and synthesis.

Literature

• Mechanistic insights into polar monomer insertion polymerization from acrylamides.

  Journal of the American Chemical Society 20120118

• Determination of the sulphoxides and sulphones of three simple sulphides in rat urine: effects of phenobarbitone, beta-naphthoflavone and methimazole.

  Biomedical chromatography : BMC 20050101