CAS 164162-36-1: 2-(tert-butyldimethylsilyl)oxyl alcohol trifluorin methanesulfonate

Description: 2-(tert-Butyldimethylsilyl)oxyl alcohol trifluoromethanesulfonate, with the CAS number 164162-36-1, is a chemical compound characterized by its unique functional groups and structural features. It contains a tert-butyldimethylsilyl group, which enhances its stability and solubility in organic solvents, making it useful in various synthetic applications. The presence of the trifluoromethanesulfonate moiety indicates that it is a strong electrophile, often employed as a leaving group in nucleophilic substitution reactions. This compound is typically used in organic synthesis, particularly in the formation of ethers and other derivatives, due to its ability to facilitate the activation of alcohols. Its reactivity profile is influenced by the electron-withdrawing nature of the trifluoromethanesulfonate group, which can enhance the electrophilicity of adjacent functional groups. Additionally, the tert-butyldimethylsilyl group can serve as a protective group for alcohols, allowing for selective reactions in multi-step synthesis. Overall, this compound is valuable in the field of organic chemistry for its versatility and reactivity.

Formula: C₉H₁₉O₄F₃SSi

Methanesulfonic acid, 1,1,1-trifluoro-, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl ester

CAS: 164162-36-1

• Formula: C₉H₁₉F₃O₄SSi
• Molecular weight: 308.3905

Everolimus Impurity 13

CAS: 164162-36-1

• Formula: C₉H₁₉F₃O₄SSi
• Molecular weight: 308.39

2-[(tert-Butyl)dimethylsiloxy]ethyl Triflate

CAS: 164162-36-1

• Formula: C₉H₁₉F₃O₄SSi
• Color and Shape: Neat
• Molecular weight: 308.39

Trifluoromethanesulfonic acid 2-[[(tert-butyl)dimethylsilyl]oxy]ethyl ester

CAS: 164162-36-1

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• Formula: C₉H₁₉F₃O₄SSi
• Purity: Min. 90%
• Molecular weight: 308.39 g/mol