CAS 54714-11-3

Thieno[3,4-d]-1,3-dioxol-2-one, 4,6-diphenyl-, 5,5-dioxide

Description:

Thieno[3,4-d]-1,3-dioxol-2-one, 4,6-diphenyl-, 5,5-dioxide is a heterocyclic organic compound characterized by its unique fused ring structure that incorporates both a thieno and dioxolane moiety. This compound features a dioxolane ring that is substituted at the 4 and 6 positions with phenyl groups, enhancing its stability and potentially influencing its reactivity. The presence of the 5,5-dioxide functional group indicates the presence of two carbonyl (C=O) functionalities, which can contribute to the compound's chemical properties, such as its ability to participate in various chemical reactions, including nucleophilic attacks. The compound is likely to exhibit interesting electronic properties due to the conjugation between the aromatic phenyl groups and the heterocyclic system. Additionally, its structural characteristics may impart specific biological activities, making it a subject of interest in medicinal chemistry. Overall, this compound's unique structure and functional groups suggest potential applications in pharmaceuticals or materials science, although specific applications would depend on further research and characterization.

Formula: C₁₇H₁₀O₅S

InChI: InChI=1S/C17H10O5S/c18-17-21-13-14(22-17)16(12-9-5-2-6-10-12)23(19,20)15(13)11-7-3-1-4-8-11/h1-10H

InChI key: InChIKey=UEOYFCIGZWQXTP-UHFFFAOYSA-N

SMILES: O=S1(=O)C(=C2C(=C1C3=CC=CC=C3)OC(=O)O2)C4=CC=CC=C4

Synonyms:

• 4,6-Diphenylenethio[3,4-d]-1,3.doxol-2-one 5,5-dioxide
• 4,6-Diphenylthieno[3,4-D][1,3]Dioxol-2-One 5,5-Dioxide
• Diphenylenethiodoxolonedioxide
• Reagents, Steglich's
• Steglich base
• Steglich's reagent
• Thieno[3,4-d]-1,3-dioxol-2-one, 4,6-diphenyl-, 5,5-dioxide

4,6-Diphenylthieno[3,4-d]-1,3-dioxol-2-one 5,5-Dioxide

CAS: 54714-11-3

Formula: C₁₇H₁₀O₅S

Purity: 98%

Molecular weight: 326.3233

Ref: IN-DA003KJW