CAS 2374-62-1

N-Ethylmethanesulfonamide

Description:

N-Ethylmethanesulfonamide is an organic compound characterized by the presence of a sulfonamide functional group, which consists of a sulfur atom bonded to a nitrogen atom and a methanesulfonyl group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is soluble in polar solvents such as water and alcohols, owing to its polar sulfonamide group. N-Ethylmethanesulfonamide is often used in organic synthesis and as a reagent in various chemical reactions, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for hydrogen bonding, which can influence its reactivity and interactions with other molecules. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance. Overall, N-Ethylmethanesulfonamide is a versatile compound with applications in both research and industry.

Formula: C₃H₉NO₂S

InChI: InChI=1S/C3H9NO2S/c1-3-4-7(2,5)6/h4H,3H2,1-2H3

InChI key: InChIKey=PZVFQOBASICMME-UHFFFAOYSA-N

SMILES: N(S(C)(=O)=O)CC

Synonyms:

• N-Ethylmethylsulfonamide
• Methanesulfonamide, N-ethyl-
• N-Ethylmethanesulfonamide

N-Ethylmethanesulfonamide

CAS: 2374-62-1

N-Ethylmethanesulfonamide is an aliphatic compound with a chemical structure containing a benzene ring and an amide group. It has analgesic properties and can be used in pharmaceutical preparations to treat pain. N-Ethylmethanesulfonamide is structurally similar to methadone, but it is not as potent. The drug binds to the opioid receptors in the brain and spinal cord, acting as a bifunctional agonist-antagonist. This binding leads to an increase in neurotransmitter release, which inhibits pain signal transmission.
N-Ethylmethanesulfonamide was first synthesized by chemists at Eli Lilly and Company in 1947. The synthesis was based on research performed by scientists at the Mayo Clinic, who were trying to create medicines for animal use that had analgesic effects similar to morphine but were less addictive than morphine itself.

Formula: C₃H₉NO₂S

Purity: Min. 95%

Molecular weight: 123.18 g/mol

Ref: 3D-CAA37462