Produktname:Tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate

IUPAC Name:tert-butyl 2-[(chlorosulfonyl)methyl]morpholine-4-carboxylate

CAS:1955506-67-8
Molekulare Formel:C10H18ClNO5S
Reinheit:95%+
Katalognummer:CM478375
Molekulargewicht:299.77

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Produkt-Details

CAS-Nr.:1955506-67-8
Molekulare Formel:C10H18ClNO5S
Schmelzpunkt:-
SMILES-Code:CC(C)(C)OC(=O)N1CCOC(CS(Cl)(=O)=O)C1
Dichte:
Katalognummer:CM478375
Molekulargewicht:299.77
Siedepunkt:
Mdl-Nr.:MFCD30181011
Lagerung:

Category Infos

Morpholines
Morpholine contains secondary amine groups and has all the typical reactive characteristics of secondary amine groups. It can react with inorganic acids to form salts, and react with organic acids to form salts or amides, which can be subjected to alkylation reaction, and can also be reacted with ethylene oxide, ketone or Willgerodt reaction. Morpholine is a six-membered ring containing oxygen and nitrogen, and its alkalinity is much lower than that of its parent piperidine. The marketed morpholine drugs are mainly distributed in the fields of tumors, cardiovascular and cerebrovascular diseases, respiratory system diseases, digestive system diseases, infectious diseases and mental disorders.
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Product Other Information

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.