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5-(iodomethyl)-3-(4-methylbenzyl)thiazolidine-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1383423-84-4

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1383423-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383423-84-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,4,2 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1383423-84:
(9*1)+(8*3)+(7*8)+(6*3)+(5*4)+(4*2)+(3*3)+(2*8)+(1*4)=164
164 % 10 = 4
So 1383423-84-4 is a valid CAS Registry Number.

1383423-84-4Downstream Products

1383423-84-4Relevant academic research and scientific papers

Synthesis of Thioalkyne-Substituted Thiazolidine-2-thiones Using Tris(triAmethylsilyl)methyllithium and Carbon Disulfide

Safa, Kazem Dindar,Alyari, Maryam

, p. 256 - 262 (2015/08/25)

An efficient, environmentally benign, and simple one-pot approach to the synthesis of 5-(iodomethyl)thiazolidine-2-thiones via multicomponent reaction of allylamines, carbon disulfide, and iodine under solvent-free conditions is presented. The obtained 5-(iodomethyl)thiazolidine-2-thiones were converted into silyl-protected-terminal [(ethynylthio)methyl]-substituted thiazolidine-2-thiones by treatment with lithium 2,2,2-tris(trimethylsilyl)ethanedithioate, produced by the reaction of tris(trimethylsilyl)methyllithium with carbon disulfide.

Synthesis of Thioalkyne-Substituted Thiazolidine-2-thiones Using Tris(trimethylsilyl)methyllithium and Carbon Disulfide

Safa, Kazem Dindar,Alyari, Maryam

, p. 256 - 262 (2015/08/25)

An efficient, environmentally benign, and simple one-pot approach to the synthesis of 5-(iodomethyl)thiazolidine-2-thiones via multicomponent reaction of allylamines, carbon disulfide, and iodine under solvent-free conditions is presented. The obtained 5-(iodomethyl)thiazolidine-2-thiones were converted into silyl-protectedterminal [(ethynylthio)methyl]-substituted thiazolidine-2-thiones by treatment with lithium 2,2,2-tris(trimethylsilyl)ethanedithioate, produced by the reaction of tris(trimethylsilyl)methyllithium with carbon disulfide.

A one-pot, three-component synthesis of thiazolidine-2-thiones

Ziyaei-Halimehjani, Azim,Marjani, Katayoun,Ashouri, Akram

, p. 3490 - 3492 (2012/08/27)

An efficient method for the synthesis of thiazolidine-2-thiones is described via regiospecific iodocyclization of an allyl amine, carbon disulfide, and iodine. Dehydrohalogenation of the iodo-derivatives gives thiazole-2(3H)-thiones. In addition, nucleoph

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