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β-Phenyl-β-trimethylsilyloxybenzenepropanoic acid ethyl ester is a complex organic compound with the molecular formula C19H24O3Si. It is a derivative of benzenepropanoic acid, featuring a β-phenyl group and a β-trimethylsilyloxy group. The ethyl ester functional group is attached to the carboxylic acid moiety, which is a common modification to improve solubility and reactivity. β-phenyl-β-trimethylsilyloxybenzenepropanoic acid ethyl ester is often used in organic synthesis, particularly in the preparation of pharmaceuticals and other specialty chemicals, due to its ability to act as a protecting group for alcohols and its potential involvement in various chemical reactions. Its structure provides a balance of steric hindrance and reactivity, making it a valuable intermediate in the synthesis of more complex molecules.

60623-96-3

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60623-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60623-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,2 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60623-96:
(7*6)+(6*0)+(5*6)+(4*2)+(3*3)+(2*9)+(1*6)=113
113 % 10 = 3
So 60623-96-3 is a valid CAS Registry Number.

60623-96-3Downstream Products

60623-96-3Relevant academic research and scientific papers

Phosphazene base-catalyzed condensation of trimethylsilylacetate with carbonyl compounds

Kobayashi, Koji,Ueno, Masahiro,Kondo, Yoshinori

, p. 3128 - 3130 (2008/09/20)

The t-Bu-P4 base was found to be an excellent catalyst for the condensation of trimethylsilylacetate or trimethylacetonitrile with carbonyl compounds to form functionalized alkenes and β-enaminoesters were also synthesized by the condensation with formanilides. The Royal Society of Chemistry 2006.

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