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Trimethylsiloxy-benzyl-methylsulphide is a complex organic compound with the chemical formula C11H20OSi. It is a colorless liquid that is soluble in organic solvents. Trimethylsiloxy-benzyl-methylsulphide is characterized by the presence of a benzyl group (C6H5CH2-), a methylsulphur group (CH3S-), and a trimethylsiloxy group (Si(OCH3)3). The trimethylsiloxy-benzyl-methylsulphide is synthesized through the reaction of benzyl bromide with sodium methylsulfide, followed by the addition of trimethylsilanol. It is used as a protecting group in organic synthesis, particularly in the preparation of pharmaceuticals and other specialty chemicals, due to its ability to shield certain functional groups from unwanted reactions while allowing others to proceed. The compound is also known for its stability and ease of removal under mild conditions, which makes it a valuable tool in the synthesis of complex molecules.

56913-04-3

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56913-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56913-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,1 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56913-04:
(7*5)+(6*6)+(5*9)+(4*1)+(3*3)+(2*0)+(1*4)=133
133 % 10 = 3
So 56913-04-3 is a valid CAS Registry Number.

56913-04-3Downstream Products

56913-04-3Relevant academic research and scientific papers

Transformation of α-assisted carbanions into the corresponding trimethylsiloxy derivatives using bis(trimethylsilyl)peroxide

Dembech,Guerrini,Ricci,Seconi,Taddei

, p. 2999 - 3006 (1990)

The reaction of bis(trimethylsilyl)peroxide with tlithium derivatives of sulphides and nitriles is reported to give the corresponding O-trimethylsilyl hemithioacetals and cyanohydrins. From these products the carbonyl function can be exposed in acidic media or in the presence of fluoride ions. This methodology provides an attractive route to transform a CH2-X group (X = PhS, MeS or CN) into the corresponding CHO, allowing the preparation of aldehydes that can be considered difficult to prepare such as, for example, formyltrimethylsilane which was generated and trapped in situ using a Wittig reaction.

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