Nombre del producto:Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate

IUPAC Name:methyl 3-(chlorosulfonyl)thiophene-2-carboxylate

CAS:59337-92-7
Fórmula molecular:C6H5ClO4S2
Pureza:97%
Número de catálogo:CM115659
Peso molecular:240.67

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CM115659-500g in stock IJůŗ
CM115659-1000g in stock ƥƿƥ

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Detalles del producto

Núm. De CAS :59337-92-7
Fórmula molecular:C6H5ClO4S2
Punto de fusión:-
Código de sonrisas:O=C(C1=C(S(=O)(Cl)=O)C=CS1)OC
Densidad:
Número de catálogo:CM115659
Peso molecular:240.67
Punto de ebullición:364.8°C at 760 mmHg
Nº Mdl:MFCD00068160
Almacenamiento:Keep in dark place, inert atmosphere, store at 2-8°C.

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.

Column Infos

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Product Other Information

Product Overview Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate (MCTC) is a sulfonated thiophene derivative that has been widely studied for its potential applications in various scientific research areas. It is a highly polar compound that has a unique chemical structure, which makes it an attractive target for synthesis and research.
Synthesis and Application Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate can be synthesized through a variety of methods, including the reaction of thiophene-2-carboxylic acid with chlorosulfonyl chloride in a solvent such as acetonitrile or dimethylformamide (DMF). This reaction is typically carried out in the presence of a base such as triethylamine or sodium hydroxide. The reaction is typically carried out at room temperature, and the desired product is obtained by crystallization or recrystallization from a suitable solvent.
Future Directions The potential future directions for research on Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate include the development of more efficient synthesis methods, the investigation of its potential applications in drug delivery, the investigation of its potential applications in the synthesis of various enzyme inhibitors, fluorescent probes and dyes, the investigation of its potential applications in the synthesis of various biologically active compounds, the investigation of its potential applications in imaging and diagnostics, the investigation of its potential applications in the treatment of various diseases, and the investigation of its potential applications in the synthesis of various pharmaceuticals.