CAS 1006381-03-8

(4R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide

Description:

(4R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide is a chemical compound characterized by its unique dioxathiolane structure, which includes a five-membered ring containing sulfur and oxygen atoms. This compound is a chiral molecule, with the (4R) designation indicating the specific stereochemistry at the fourth carbon atom. It typically exhibits properties associated with dioxathiolanes, such as potential reactivity in nucleophilic substitution reactions due to the presence of the sulfur atom. The dioxathiolane ring contributes to its stability and may influence its solubility in various solvents. Additionally, this compound may have applications in organic synthesis or as an intermediate in the production of other chemical entities. Its specific interactions and reactivity can be influenced by the presence of the methyl group, which can affect steric hindrance and electronic properties. As with many sulfur-containing compounds, it may also exhibit unique odor characteristics. Safety data and handling precautions should be consulted, as with any chemical substance, to ensure proper usage and risk management.

Synonyms:

• 1,3,2-Dioxathiolane, 4-Methyl-, 2,2-dioxide, (4R)-
• (R)-4-Methyl-1,3,2-Dioxathiolane2,2-Dioxide
• (R)-4-methyl-1,3,2-dioxathiolane 2,2-dioxide

1,3,2-Dioxathiolane, 4-methyl-, 2,2-dioxide, (4R)-

CAS: 1006381-03-8

Formula: C₃H₆O₄S

Purity: 98%

Color and Shape: Liquid

Molecular weight: 138.1423

Ref: IN-DA008WVA

(4R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide

CAS: 1006381-03-8

(4R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide

Formula: C₃H₆O₄S

Purity: 99%

Color and Shape: Liquid

Molecular weight: 138.14g/mol

Ref: 54-OR305470

(R)-4-Methyl-1,3,2-dioxathiolane 2,2-dioxide

CAS: 1006381-03-8

Purity: 98%

Color and Shape: Liquid

Molecular weight: 138.1399994

Ref: 10-F615589

(4R)-4-Methyl-1,3,2-dioxathiolane-2,2-dioxide

Controlled Product

CAS: 1006381-03-8

Applications (4R)-4-Methyl-1,3,2-dioxathiolane-2,2-dioxide, can be used in the synthesis of stereoisomers of Secnidazole (S225000), which is a nitroimidazole anti-infective, that is shown to be effective in treatment of dientamoebiasis, and Atopobium vaginae.
References De Backer, E. et al.: Clinc. Micro. Infec., 16, 470 (2009); Cosar, C., et al.: Arzneim.-Forsch., 16, 23 (1966); Videau, D., et al.: Br. J. Vener. Dis., 54, 77 (1978); Symonds, J., et al.: J. Antimicrob. Chemother., 5, 484 (1979);

Formula: C₃H₆O₄S

Color and Shape: Neat

Molecular weight: 138.142

Ref: TR-M303700