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88733-61-3

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88733-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88733-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,3 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88733-61:
(7*8)+(6*8)+(5*7)+(4*3)+(3*3)+(2*6)+(1*1)=173
173 % 10 = 3
So 88733-61-3 is a valid CAS Registry Number.

88733-61-3Downstream Products

88733-61-3Relevant academic research and scientific papers

Ligand exchange reaction of sulfoxides in organic synthesis: A novel method for synthesizing acetylenes and allenes from carbonyl compounds through sulfoxides having a trifluoromethanesulfonyloxy group on the β-carbon

Satoh, Tsuyoshi,Itoh, Norifumi,Watanabe, Shizue,Koike, Hirofumi,Matsuno, Haruko,Matsuda, Kenji,Yamakawa, Koji

, p. 9327 - 9338 (2007/10/02)

A novel method for synthesizing acetylenes and allenes from carbonyl compounds is described. Ligand exchange reaction of alkenylsulfoxides having a trifluoromethanesulfonyloxy group on the β-carbon, which were derived from α-alkyl β-ketosulfoxides, with n

Ligand Exchange Reaction of Sulfoxides in Organic Synthesis. A Novel Method for Synthesizing Acetylenes from Carbonyl Compounds through β-Trifluoromethanesulfonyloxy Vinyl Sulfoxides

Satoh, Tsuyoshi,Itoh, Norifumi,Watanabe, Shizue,Matsuno, Haruko,Yamakawa, Koji

, p. 567 - 570 (2007/10/02)

α-Sulfinyl ketones were prepared by the reaction of alkyl phenyl sulfoxide or chloromethyl p-tolyl sulfoxide with aldehydes or methyl esters in high yields, and were converted to acetylenes through β-trifluoromethanesulfonyloxy vinyl sulfoxides by the lig

A CONVENIENT SYNTHESIS OF UNSYMMETRICAL BIBENZYLS, HOMOALLYLARENES, AND HOMOPROPARGYLARENES VIA PALLADIUM-CATALYZED CROSS COUPLING

Negishi, Ei-ichi,Matsushita, Hajime,Kobayashi, Makoto,Rand, Cynthia L.

, p. 3823 - 3824 (2007/10/02)

The palladium-catalyzed homobenzyl-aryl, homobenzyl-alkenyl, homoallyl-aryl, and homopropargyl-aryl cross coupling reactions provide the desired coupling products in high yields, whereas similar reactions involving akynyl halides lead to low product yields.

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