CAS 96013-95-5

Benzaldehyde, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

Description:

Benzaldehyde, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]- is an organic compound characterized by its structure, which includes a benzaldehyde moiety substituted with a silyl ether group. The presence of the dimethylsilyl group enhances its stability and solubility in organic solvents. This compound typically exhibits a pleasant almond-like aroma, characteristic of benzaldehyde derivatives. It is generally a colorless to pale yellow liquid at room temperature and has a relatively low boiling point compared to many other organic compounds. The silyl ether functionality can provide unique reactivity, making it useful in various synthetic applications, particularly in organic synthesis and as a protecting group in chemical reactions. Additionally, the compound may exhibit moderate volatility and can be sensitive to moisture, which is a common trait among silyl compounds. Safety precautions should be taken when handling this substance, as it may pose health risks if inhaled or ingested. Overall, its unique structural features contribute to its utility in chemical research and industrial applications.

Formula: C₁₃H₂₀O₂Si

3-((tert-Butyldimethylsilyl)oxy)benzaldehyde

CAS: 96013-95-5

3-((tert-Butyldimethylsilyl)oxy)benzaldehyde

Purity: 98%

Ref: 54-OR1041119

3-((tert-Butyldimethylsilyl)oxy)benzaldehyde

CAS: 96013-95-5

Purity: 98%

Molecular weight: 236.3860016

Ref: 10-F764913

3-tert-Butyldimethylsilyloxybenzaldehyde

Controlled Product

CAS: 96013-95-5

Formula: C₁₃H₂₀O₂Si

Color and Shape: Neat

Molecular weight: 236.39

Ref: TR-B693375

3-tert-Butyldimethylsilyloxybenzaldehyde

CAS: 96013-95-5

3-tert-Butyldimethylsilyloxybenzaldehyde is a synthetic opioid that has been used in the screening of opioid receptor targets. It is soluble in organic solvents, such as chloroform and ether, with a melting point of about -30°C. 3-tert-Butyldimethylsilyloxybenzaldehyde has been shown to have analgesic activity in mice at low doses. The analgesic effect is due to stimulation of μ opioid receptors. In addition, this compound also has the ability to inhibit amide formation with low temperatures. 3-tert-Butyldimethylsilyloxybenzaldehyde can be synthesized by alkylation or derivatization of benzyl alcohol or benzyl chloride. It can also be obtained through the condensation of 2,6-dimethylaniline with acetone followed by reduction with lithium aluminum hydride or sodium borohydride.

Formula: C₁₃H₂₀O₂Si

Purity: Min. 95%

Molecular weight: 236.38 g/mol

Ref: 3D-WDA01395