CAS 10512-65-9

2H-1,3-Benzothiazine-2,4(3H)-dione

Description:

2H-1,3-Benzothiazine-2,4(3H)-dione, also known as benzothiazine dione, is a heterocyclic compound characterized by its fused benzene and thiazine rings, which contribute to its unique chemical properties. This compound typically exhibits a solid state at room temperature and is known for its stability under standard conditions. It features a dione functional group, which imparts reactivity, particularly in nucleophilic addition reactions. The presence of the thiazine ring enhances its potential for biological activity, making it of interest in medicinal chemistry. Its solubility can vary depending on the solvent, and it may exhibit moderate polarity due to the functional groups present. Additionally, 2H-1,3-Benzothiazine-2,4(3H)-dione can participate in various chemical reactions, including oxidation and reduction processes, which are relevant in synthetic organic chemistry. Overall, this compound's structural characteristics and functional groups make it a valuable subject of study in both organic synthesis and pharmacology.

Formula: C₈H₅NO₂S

2H-Benzo[e][1,3]thiazine-2,4(3H)-dione

CAS: 10512-65-9

Purity: 98%

Molecular weight: 179.1900024

Ref: 10-F614898

3,4-Dihydro-2H-1,3-benzothiazine-2,4-dione

CAS: 10512-65-9

Versatile small molecule scaffold

Formula: C₈H₅NO₂S

Purity: Min. 95%

Molecular weight: 179.2 g/mol

Ref: 3D-KAA51265