925446

5-Vinylthianthrenium tetrafluoroborate

≥95%

• Sinônimo(s): Vinyl-TT
• Fórmula empírica (Notação de Hill): C₁₄H₁₁BF₄S₂
• Número CAS: 2703016-98-0
• Peso molecular: 330.17
• Número MDL: MFCD34622433
• Código UNSPSC: 12352108
• NACRES: NA.22

Propriedades

• Nível de qualidade: 100
• Ensaio: ≥95%
• Formulário: powder
• adequação da reação: reaction type: C-C Bond Formation
• pf: 110-112 °C
• grupo funcional: thioether
• temperatura de armazenamento: −20°C
• cadeia de caracteres SMILES: [F-][B+3]([F-])([F-])[F-].S1C=2C=CC=CC2[S+](C=C)C=3C=CC=CC13
• InChI: 1S/C14H11S2.BF4/c1-2-16-13-9-5-3-7-11(13)15-12-8-4-6-10-14(12)16;2-1(3,4)5/h2-10H,1H2;/q+1;-1
• chave InChI: FXHBWPNFHMRFKM-UHFFFAOYSA-N

Descrição

Aplicação

5-Vinylthianthrenium tetrafluoroborate is a crystalline, shelf-stable vinylating reagent developed by the Ritter Lab. Despite the great functionality of the vinyl group for diversification of target compounds, the selective installation of this moeity has remained challenging. 5-Vinylthianthrenium tetrafluoroborate can perform this otherwise challenging transformation with a broad scope of substrate, including the N-vinylation of heterocycles, vinylation of aryl boronic acids, and the annulation of cyclic and heterocyclic substrates. Additionally, this reagent can be used to enable palladium catalyzed cross-coupling reactions. The functionality of 5-vinylthianthrenium tetrafluoroborate enables the usage of vinyl groups as a versatile tool for further functionalization of many substrates and is a functional tool for many snythetic pathways.

Outras notas

Chemoselective umpolung of thiols to episulfoniums for cysteine bioconjugation

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable