Produktname:Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate
IUPAC Name:tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate
Product Overview |
Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate (CMC) is a chemical compound that has gained significant attention in the field of scientific research. CMC is a versatile molecule that has shown promise in various applications, including as a reagent in organic synthesis and as a tool for investigating biological systems. |
Synthesis and Application |
The synthesis of Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate involves the reaction of tert-butyl 4-hydroxymethylmorpholine-2-carboxylate with chlorosulfonyl isocyanate. The reaction takes place in the presence of a base, such as triethylamine, and a solvent, such as dichloromethane. The resulting product is a white solid that can be purified by recrystallization or chromatography. Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate has been used in various scientific research applications, including as a reagent in organic synthesis and as a tool for investigating biological systems. In organic synthesis, Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate has been used as a protecting group for carboxylic acids and as a reagent for the synthesis of β-lactams and γ-lactones. In biological systems, Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate has been used as a tool for investigating the role of sulfonate esters in enzyme-catalyzed reactions and as a probe for investigating the structure and function of ion channels. |
Future Directions |
There are several future directions for research on Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate. One direction is to investigate the mechanism of action of Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate in more detail. This could involve using Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate as a tool to investigate the role of sulfonate esters in enzyme-catalyzed reactions and ion channel function. Another direction is to explore the potential therapeutic applications of Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate. For example, Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate could be used as a tool for developing new drugs that target sulfonate ester-metabolizing enzymes or ion channels. Finally, future research could focus on developing new synthetic routes for Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate that are more efficient and environmentally friendly. |