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Trimethylsilyl 4-methyldithiobenzoate is a chemical compound with the molecular formula C11H14OS2Si. It is a colorless to pale yellow liquid and is used as a protecting group in organic synthesis, particularly for thiols. The compound is characterized by its ability to form a stable, less reactive derivative of thiols, which can be deprotected under mild conditions. This property makes it valuable in the synthesis of complex organic molecules where thiol groups need to be temporarily masked. The compound is also known for its stability and ease of synthesis, which contributes to its utility in various chemical reactions.

42967-56-6

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42967-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42967-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,6 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42967-56:
(7*4)+(6*2)+(5*9)+(4*6)+(3*7)+(2*5)+(1*6)=146
146 % 10 = 6
So 42967-56-6 is a valid CAS Registry Number.

42967-56-6Downstream Products

42967-56-6Relevant articles and documents

The Preparation and Some Reactions of Unsymmetrical Acyl Thioacyl Sulfides

Kato, Shinzi,Sugino, Katsumi,Matsuzawa, Yukihiko,Katada, Tomonori,Noda, Ippei,et al.

, p. 1798 - 1811 (2007/10/02)

A number of unsymmetrical acyl thioacyl sulfides have been prepared and characterized by the reaction of piperidinium or sodium dithiocarboxylates with acyl chlorides or by desulfurization reaction of acyl thioacyl disulfides with triphenylphosphine.They are deep blue oils or light green crystals and very unstable thermally and for moisture.The n --> ?* transitions of the thiocarbonyl group of 1 appear in higher wave length region than those of the corresponding symmetrical bis(thioacyl) sulfides .Some reactions with nucleophiles are discussed.It was found that the symmetricallization reaction of these unsymmetrical acyl thioacyl sulfides occurs in the presence of base such as lithium ethanethiolate to give the symmetrical bis(thioacyl) disulfides in fair yield.

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