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1-Methylmercapto-1,2-diphenyl-aethylen, also known as 1-Methylthio-1,2-diphenylethylene, is an organic compound characterized by its unique chemical structure. It features a phenylethylene backbone with a methylthio (methylmercapto) group attached to the terminal carbon atom. This molecule is composed of a carbon-carbon double bond, two phenyl rings, and a methylmercapto group, which contributes to its distinct chemical properties. The compound is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and materials due to its specific reactivity and structural features.

4843-36-1

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4843-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4843-36-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4843-36:
(6*4)+(5*8)+(4*4)+(3*3)+(2*3)+(1*6)=101
101 % 10 = 1
So 4843-36-1 is a valid CAS Registry Number.

4843-36-1Downstream Products

4843-36-1Relevant academic research and scientific papers

NEW PERSPECTIVE FOR THE SYNTHETIC APPLICATION OF SOME α-SULFENYLATED BENZYLIC SULFONES, SYNTHESIS OF VINYL SULFIDES.

Wladislaw, Blanka,Marzorati, Liliana,Zaim, Marcio H.

, p. 329 - 330 (2007/10/02)

Some α-sulfenylated para-substituted benzylic sulfones, obtained by sulfenylation of the corresponding sulfones, were submitted to reaction with CCl4-KOH-t-BuOH to give the corresponding para-substituted α-methylthio-dimethyl styrenes.

REACTIVE DOUBLE BOND SYSTEMS VIA (3+2) CYCLOREVERSION OF HETEROCYCLES

Schaumann, Ernst

, p. 995 - 1008 (2007/10/02)

After deprotonation, saturated five-membered heterocyclic rings give a facile (3+2) cycloreversion.This approach is employed in syntheses of ketenes, thioaldehydes, thioketones, thioketenes and a thioquinone at low temperature.These highly reactive double-bond systems are usually trapped in situ using (2+2), (2+3), or (2+4) cycloadditions to give various types of heterocycles.

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