Benzaldehyde, 4-(trimethylsilyl)-, also known by its CAS number 2199-32-8, is an organic compound characterized by the presence of a benzaldehyde moiety substituted with a trimethylsilyl group at the para position. This compound typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. It is relatively non-polar due to the presence of the trimethylsilyl group, which enhances its solubility in organic solvents while making it less soluble in water. The trimethylsilyl group can also serve as a protective group in organic synthesis, facilitating various reactions such as nucleophilic substitutions and eliminations. Benzaldehyde derivatives are often utilized in the synthesis of fragrances, pharmaceuticals, and agrochemicals. The compound is stable under normal conditions but should be handled with care due to potential irritant properties. Its reactivity can be influenced by the presence of the silyl group, making it a valuable intermediate in synthetic organic chemistry.

Benzaldehyde,4-(trimethylsilyl)-

2199-32-8: Benzaldehyde,p-(trimethylsilyl)- (6CI,7CI,8CI), 4-(Trimethylsilyl)benzaldehyde, p-(Trimethylsilyl)benzaldehyde

4-(Trimethylsilyl)benzaldehyde

4-(Trimethylsilyl)benzaldehyde is an undescribed monomer that has been synthesized in the laboratory. It is a centrosymmetric molecule with three phenyl groups and a silicon atom, which are connected by sulfonation. 4-(Trimethylsilyl)benzaldehyde can be used as a precursor to produce amines and covid-19 pandemic. The synthesis of 4-(trimethylsilyl)benzaldehyde can be regiospecifically achieved through chlorination, although this method is not efficient. The carbonyl group in this molecule can be used as part of a catalytic process for the synthesis of carbazones.

CAS 2199-32-8: Benzaldehyde,4-(trimethylsilyl)-

4-(Trimethylsilyl)benzaldehyde

Ref: 10-F602169

4-(Trimethylsilyl)benzaldehyde

Ref: 3D-CAA19932

4-(Trimethylsilyl)benzaldehyde

Ref: 54-OR931092