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Trithiocarbonic acid monobenzyl ester, also known as benzyl trithiocarbonate, is an organosulfur compound with the chemical formula C8H8OS3. It is a colorless to pale yellow liquid that is soluble in organic solvents and has a pungent odor. trithiocarbonic acid monobenzyl ester is formed by the esterification of trithiocarbonic acid with benzyl alcohol, resulting in a molecule that contains three sulfur atoms bonded to a central carbon atom, with a benzyl group attached to one of the sulfur atoms. Trithiocarbonic acid monobenzyl ester is primarily used as a reagent in organic synthesis, particularly in the preparation of various sulfur-containing compounds. It is also employed as a vulcanization accelerator in the rubber industry and as a fungicide in agriculture. Due to its reactivity and potential health risks, it is important to handle this chemical with care, following proper safety protocols.

66728-36-7

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66728-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66728-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,2 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66728-36:
(7*6)+(6*6)+(5*7)+(4*2)+(3*8)+(2*3)+(1*6)=157
157 % 10 = 7
So 66728-36-7 is a valid CAS Registry Number.

66728-36-7Relevant articles and documents

Facile one pot synthesis of a range of reversible addition-fragmentation chain transfer (RAFT) agents

Skey, Jared,O'Reilly, Rachel K.

supporting information; experimental part, p. 4183 - 4185 (2009/03/11)

The application of a universal synthetic strategy for the high yielding and facile synthesis of a wide range of functional RAFT agents including trithiocarbonates, xanthates and dithiocarbamates is described. The Royal Society of Chemistry.

Synthesis and reactions of 2-(alkylthio)-4,4-dimenthyl-1,3-thiazole-5(4H)-thiones

Shi,Linden,Heimgartner

, p. 1903 - 1920 (2007/10/02)

Six 2-(alkylthio)-substituted 4,4-dimethyl-1,3-thiazole-5(4H)-thiones were synthesized according to a new method. The reactions of these compounds with allyl- and benzyllithium reagents, 1,3-dipoles, and dimethyl acetylenedicarboxylate proceeded in a similar manner to 2-alkyl-substituted analogues, while methyllithium reacted in a different way yielding trithio-orthoester derivatives.

SYNTHESIS, STRUCTURE, AND REACTIONS OF THIOCARBONIC ACID DERIVATIVES NEW PENTATHIODIPERCARBONATES, (RSS)2C=S, α,α,α-TRIS(DISULFIDES), AND THE FIRST α,α,α-TRIS(TRISULFIDE)

Hansen, Holger C.,Senning, Alexander,Hazell, Rita G.

, p. 5145 - 5158 (2007/10/02)

Novel bis(perhaloalkyl) pentathiodipercarbonates 5b-d have been synthesised by reaction of sulfenyl chlorides with metal trithiocarbonates, and the heptathio analog 21a was prepared similarly.Lenthionine 19 is the main product when diiodomethane is treated with sodium tetrathiopercarbonate.A rearrangement of bis(alkyltrithio)dichloromethanes 24 has been observed.Additions of sulfenyl chlorides and of thiosulfenyl chlorides to the thiocarbonyl compounds 5 and 21a were achieved in acetonitrile.The structures of the first crystalline pentathiodipercarbonate 5a and α,α,α-tris(disulfide) 29a, and of the first reported α,α,α-tris(trisulfide) 31a have been determined by X-ray crystallography.

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