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α-Hydroxy-α-trimethylsilylethylbenzene is an organic compound characterized by its unique structure, which features a benzene ring with an ethyl group attached to the α-carbon, which in turn is bonded to a trimethylsilyl group and a hydroxyl group. α-hydroxy-α-trimethylsilylethylbenzene is known for its stability and reactivity, which can be attributed to the electron-donating nature of the trimethylsilyl group and the presence of the hydroxyl group, making it a versatile building block in organic synthesis. It is often used in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its ability to participate in a range of chemical reactions, such as nucleophilic substitutions and condensations. The compound's properties also make it a subject of interest in research for new applications in materials science and chemical engineering.

53173-00-5

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53173-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53173-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53173-00:
(7*5)+(6*3)+(5*1)+(4*7)+(3*3)+(2*0)+(1*0)=95
95 % 10 = 5
So 53173-00-5 is a valid CAS Registry Number.

53173-00-5Relevant academic research and scientific papers

Rhodium-catalyzed arylation of acylsilanes with sodium tetraarylborates

Matsuda, Takanori,Mizuno, Kohei,Watanuki, Shoichi

supporting information, p. 64 - 67 (2014/06/09)

Rhodium(I)-catalyzed arylation of benzoylsilanes with sodium tetraarylborates affords α-silyl benzhydrols, benzhydryl silyl ethers, benzhydrols, and diaryl ketones selectively depending on the catalyst, solvent, and temperature.

Mg-promoted reductive coupling of aromatic carbonyl compounds with trimethylsilyl chloride and bis(chlorodimethylsilyl) compounds

Uchida, Tetsuro,Kita, Yoshio,Maekawa, Hirofumi,Nishiguchi, Ikuzo

, p. 3103 - 3111 (2007/10/03)

Mg-promoted reductive coupling of aromatic carbonyl compounds (1) with chlorosilanes, such as trimethylsilyl chloride (TMSCl:2), 1,2- bis(chlorodimethylsilyl)ethane (3) and 1,5-dichlorohexamethyltrisiloxane (4), in N,N-dimethylformamide (DMF) at room temperature brought about selective and facile reductive formation of both of carbon-silicon and oxygen-silicon bonds to give the corresponding α-trimethylsilylalkyl trimethylsilyl ethers (5) and cyclic siloxanes (6), (7) in moderate to good yields, respectively. The present facile and selective coupling may be initiated through electron transfer from Mg metal to aromatic carbonyl compounds (1).

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