cas 2092286-66-1|| where to buy 2,2-dioxo-2lambda6-thiaspiro[3.3]heptane-6-carboxylic acid

Nombre del producto:2,2-dioxo-2lambda6-thiaspiro[3.3]heptane-6-carboxylic acid

IUPAC Name:2,2-dioxo-2λ⁶-thiaspiro[3.3]heptane-6-carboxylic acid

: CAS：2092286-66-1; Fórmula molecular：C7H10O4S; Pureza：95%+

: Número de catálogo：CM462595; Peso molecular：190.21

Unidad de embalaje	Stock disponible	Precio($)
CM462595-100mg	in stock	ŭňș
CM462595-250mg	in stock	ƅňƩ

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Detalles del producto

: Núm. De CAS :2092286-66-1; Fórmula molecular:C7H10O4S; Punto de fusión:-; Código de sonrisas:OC(=O)C1CC2(C1)C[S](=O)(=O)C2; Densidad:

: Número de catálogo:CM462595; Peso molecular:190.21; Punto de ebullición:; Nº Mdl:MFCD30635373; Almacenamiento:

Category Infos

: Cyclobutanes; The molecular structure of cyclobutane has four carbon atoms, and its four carbon atoms are not in the same plane, which is the folded conformation of cyclobutane. Cyclobutane itself is not of commercial or biological interest, but more complex derivatives are important in biology and biotechnology. Currently, nine FDA-approved drugs contain the cyclobutane structure. From the perspective of therapeutic areas, cyclobutyl drugs are mainly distributed in popular areas such as tumors, neurological diseases, infectious diseases, endocrine and metabolic diseases.

: Thietanes; Thietanes are important structural motifs of some biological compounds and useful intermediates in organic synthesis.

Product Other Information

Product Overview

2,2-Dioxo-2lambda6-thiaspiro[3.3]heptane-6-carboxylic acid is a sulfur-containing Spiro compound that has been extensively studied for its potential applications in various fields of science, including medicinal chemistry, biochemistry, and material science. This compound is synthesized through a multi-step process, and its unique structure and properties make it an attractive target for further investigation.

Synthesis and Application

2,2-Dioxo-2lambda6-thiaspiro[3.3]heptane-6-carboxylic acid has been extensively studied for its potential applications in medicinal chemistry. It has been reported to exhibit a wide range of biological activities, including antibacterial, antifungal, and anticancer properties. 2,2-Dioxo-2lambda6-thiaspiro[3.3]heptane-6-carboxylic acid has been shown to inhibit the growth of various bacterial and fungal strains, including drug-resistant strains. It has also been reported to induce apoptosis in cancer cells, making it a potential candidate for cancer therapy.