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3-(phenylthio)-1,3-pentadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69063-45-2

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69063-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69063-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,6 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69063-45:
(7*6)+(6*9)+(5*0)+(4*6)+(3*3)+(2*4)+(1*5)=142
142 % 10 = 2
So 69063-45-2 is a valid CAS Registry Number.

69063-45-2Relevant academic research and scientific papers

Synthesis and Applications of 3-Phenylthio-2-sulfolenes

Chou, Shang-Shing P.,Chao, Mao-Hsun

, p. 53 - 59 (1996)

Treatment of 3-phenylthio-2-sulfolene (1) with an equimolar proportion of butyllithium at -78 °C in THF followed by addition of an electrophile gave the 2-substituted 3-phenylthio-2-sulfolenes (2). The deprotonation was found to proceed only at the vinylic C-2 position. Some of the 2-sulfolenes 2 underwent desulfonylation upon heating with base. Of particular interest was the conversion of 3-phenylthio-2-trimethylsilyl-2-sulfolene (2h) to its 3-sulfolene isomer 6 by sequential addition of butyllithium and salicylic acid at low temperatures. The 3-sulfolene 6 was desulfonylated by Kugelrohr distillation at 150 °C under vacuum to give (Z)-2-phenylthio-1-trimethylsilyl-1,3-butadiene (8). The regiochemistry of the Diels Alder reaction of this highly reactive diene 8 was found to be controlled by the phenylthio group, and the stereochemistry is endo addition. Diene 8 was oxidized to its sulfone derivative 12 which also underwent a stereospecific Diels-Alder reaction.

Synthesis and applications of tetrahydro-2-pyridinones via aza-Diels - Alder reactions of thio-substituted 1,3-dienes with arylsulfonyl isocyanates

Chou,Hung

, p. 2450 - 2462 (2007/10/03)

The first aza-Diels - Alder reactions of arylsulfonyl isocyanates with thio-substituted 1,3-dienes via the 3-sulfolene precursors 1 gave the cyclized products 3 with complete control of chemo- and regioselectivity. The cyclized products 3a and 5 underwent further reactions with nucleophiles and bases to give useful heterocyclic compounds. The N-tosyl group of the cyclic products could be selectively replaced by hydrogen or another substituent.

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