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Trimethyl(1-(phenylthio)pentyl)silane is an organosilicon compound characterized by its molecular formula C14H24SSi. It features a trimethylsilyl group (SiMe3) attached to a pentyl chain, which is further substituted with a phenylthio group (C6H5S) at the terminal end. This chemical is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-sulfur bonds and as a protecting group for thiols. Its unique structure allows it to participate in various chemical reactions, making it a valuable tool in the field of organic chemistry.

76200-37-8

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76200-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76200-37-8 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, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76200-37:
(7*7)+(6*6)+(5*2)+(4*0)+(3*0)+(2*3)+(1*7)=108
108 % 10 = 8
So 76200-37-8 is a valid CAS Registry Number.

76200-37-8Relevant academic research and scientific papers

Strategic Trimethylsilyldiazomethane Insertion into pinB-SR Followed by Selective Alkylations

Civit, Marc G.,Royes, Jordi,Vogels, Christopher M.,Westcott, Stephen A.,Cuenca, Ana B.,Fernández, Elena

, p. 3830 - 3833 (2016/08/16)

The insertion of the diazo derivative Me3SiCHN2 into pinB-SR σ bonds (R = Ph, Tol, Bn) allows a direct synthesis of multisubstituted H-C(SR)(Bpin)(SiMe3) compounds. Consecutive base-assisted transformations of HC(S)(B) (Si

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).

A NEW METHOD FOR PREPARING 1-PHENYLTHIO-1-TRIMETHYLSILYLALKANES: THE PREPARATION OF α-SILYLCARBANIONS AND OLEFINS.

Ager, David J.

, p. 2923 - 2926 (2007/10/02)

1-Phenylthio-1-trimethylsilylalkanes(1) are prepared in high yield from 1,1-bis(phenylthio)acetals(2) by reaction with lithium naphthalenide(3) followed by chlorotrimethylsilane. α-Silylcarbanions are formed from the alkanes(1) and lithium naphthalenide(3).Subsequent reaction with carbonyl compounds gave the olefins(4) via the Peterson reaction.

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