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Trimethylsilyl phenyl thioketone is a chemical compound with the molecular formula C9H12OSi. It is a colorless liquid that is soluble in organic solvents. trimethylsilyl phenyl thioketone is characterized by the presence of a phenyl group (C6H5) attached to a thioketone moiety, which consists of a carbonyl group (C=O) bonded to a sulfur atom. The trimethylsilyl group (Si(CH3)3) is attached to the thioketone, providing stability and reactivity to the molecule. Trimethylsilyl phenyl thioketone is used as a reagent in organic synthesis, particularly in the formation of carbon-sulfur bonds and as a protecting group for thiols. It is also employed in the synthesis of various pharmaceuticals and agrochemicals due to its ability to modify the reactivity and selectivity of certain reactions.

79841-55-7

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79841-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79841-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,4 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79841-55:
(7*7)+(6*9)+(5*8)+(4*4)+(3*1)+(2*5)+(1*5)=177
177 % 10 = 7
So 79841-55-7 is a valid CAS Registry Number.

79841-55-7Upstream product

79841-55-7Relevant academic research and scientific papers

Cobalt(II) Chloride Promoted Thionation of Carbonyl Compounds: A Simple Access to Silyl Thioketones and Thioaldehydes

Ricci, Alfredo,Degl'Innocenti, Alessandro,Capperucci, Antonella,Reginato, Gianna

, p. 19 - 20 (2007/10/02)

The CoCl2-catalyzed reaction of Me3SiSSiMe3 with acylsilanes and simple aldehydes affords a direct and easy entry to their sulfur analogues.

Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides

Barbaro, Gaetano,Battaglia, Arturo,Giorgianni, Patrizia,Maccagnani, Gaetano,Macciantelli, Dante,et al.

, p. 381 - 386 (2007/10/02)

Trimethylsilyl and triphenylsilylaryl thioketones have been synthesized by acid catalysed reaction of the corresponding ketones with hydrogen sulphide.Such silylated thioketones heve been oxidized to give S-oxides and converted with diaryldiazomethanes into triaryl thiiranes; upon treatment with organolithium nucleophiles they undergo thiophilic addition.The ready desulphurization with triphenylphosphine of silylated thiirans to the corresponding silyl triaryl ethylenes is also reported.

Silyl Thioketones and Silylated Thiirans

Bonini, Bianca F.,Mazzanti, Germana,Sarti, Sauro,Zanirato, Paolo,Maccagnani, Gaetano

, p. 822 - 823 (2007/10/02)

The preparation of silyl thioketones, and their reactions leading to silylated thiirans and other hitherto unknown silylated heterocycles, are reported.

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