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Trimethyl-(2-methyl-1-phenylsulfanyl-butoxy)-silane is a complex organic compound with the chemical formula C14H23OSi. It is a colorless liquid at room temperature and is soluble in organic solvents. Trimethyl-(2-methyl-1-phenylsulfanyl-butoxy)-silane is characterized by a silicon atom bonded to three methyl groups and a butoxy group, which is further connected to a 2-methyl-1-phenylsulfanyl butane moiety. The presence of the phenylsulfanyl group gives it unique properties, making it potentially useful in various chemical reactions and applications, such as in the synthesis of organosilicon compounds or as a reagent in organic synthesis. Due to its specific structure, it may also have applications in materials science or as a precursor in the production of specialty chemicals.

76200-52-7

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76200-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76200-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,0 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76200-52:
(7*7)+(6*6)+(5*2)+(4*0)+(3*0)+(2*5)+(1*2)=107
107 % 10 = 7
So 76200-52-7 is a valid CAS Registry Number.

76200-52-7Relevant academic research and scientific papers

A NEW METHOD FOR CONVERTING ALKYL HALIDES TO HOMOLOGOUS ALDEHYDES

Ager, David J.,Cookson, Richard C.

, p. 1677 - 1680 (1980)

Phenylthiotrimethylsilylmethyl lithium can be alkylated and the product hydrolysed to the aldehydes by oxidation and rearrangement.

Synthesis of Aldehydes from Phenylthiotrimethylsilylmethane

Ager, David J.

, p. 1131 - 1136 (2007/10/02)

Phenylthiotrimethylsilylmethyl-lithium (4) reacts with alkyl halides to give 1-phenylthio-1-trimethylsilylalkanes (5), which can also be prepared by the addition of alkyl-lithium to 1-phenylthio-1-trimethylsilylethene (8), or from bis(phenylthio)acetals (11).The 1-phenylthio-1-trimethylsilylalkanes (5) can be converted into the corresponding aldehyde (15) by oxidation to the sulphoxide (13), thermal rearrangement, and hydrolysis of the resultant O-silyl thioacetal (14).

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