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Trimethyl-((1Z,3E)-2-methyl-1-phenyl-penta-1,3-dienyloxy)-silane is a complex organic compound with the molecular formula C15H22OSi. It is a colorless liquid at room temperature and is characterized by its unique structure, which includes a trimethylsilyl group attached to a conjugated diene system with a phenyl group. Trimethyl-((1Z,3E)-2-methyl-1-phenyl-penta-1,3-dienyloxy)-silane is primarily used as a protecting group in organic synthesis, particularly for alcohols, due to its stability and ease of removal under mild conditions. It is also known for its applications in the synthesis of various organic compounds, such as natural products and pharmaceuticals, where selective protection of functional groups is crucial. The compound's reactivity and selectivity make it a valuable tool in the field of organic chemistry.

87514-18-9

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87514-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87514-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,1 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87514-18:
(7*8)+(6*7)+(5*5)+(4*1)+(3*4)+(2*1)+(1*8)=149
149 % 10 = 9
So 87514-18-9 is a valid CAS Registry Number.

87514-18-9Relevant academic research and scientific papers

AN EFFICIENT SYMTHESIS OF SILYL ENOL ETHERS FROM α,β-UNSATURATED ALDEHYDES AND KETONES

Iqbal, Javed,Khan, M. Amin

, p. 515 - 522 (2007/10/02)

α,β-Unsaturated aldehydes and ketones when reacted with NaBr-Me3SiCl-Et3N in DMF at ambient temperature, yield silyl dienol ethers in high yields.

α:γ RATIOS IN PHENYLTHIOMETHYLATION OF SILYL DIENOL ETHERS

Fleming, Ian,Iqbal, Javed

, p. 2913 - 2916 (2007/10/02)

We report α:γ ratios for the electrophilic attack of phenylthiomethyl chloride on all the possible 2- and 4-methylated 1-phenyl-1-trimethylsilyloxybutadienes (7a-7e); the methyl groups appear to reduce the proportion of attack taking place at the carbon atom carrying the methyl groups.

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