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ethyl 4,5-dihydro-2,4-diphenyl-3-furancarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34878-89-2

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34878-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34878-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,7 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34878-89:
(7*3)+(6*4)+(5*8)+(4*7)+(3*8)+(2*8)+(1*9)=162
162 % 10 = 2
So 34878-89-2 is a valid CAS Registry Number.

34878-89-2Downstream Products

34878-89-2Relevant academic research and scientific papers

Reaction of Corey ylide with α,β-Unsaturated Ketones: Tuning of Chemoselectivity toward Dihydrofuran Synthesis

Chagarovsky, Alexey O.,Budynina, Ekaterina M.,Ivanova, Olga A.,Villemson, Elena V.,Rybakov, Victor B.,Trushkov, Igor V.,Melnikov, Mikhail Ya.

supporting information, p. 2830 - 2833 (2014/06/23)

A straightforward, efficient, and reliable approach to synthetically valuable 2,3-dihydrofurans via a reaction between Corey ylide and α,β-unsaturated ketones has been developed. The use of simple and widely spread starting materials as well as mild reaction conditions and scalability provide a broad scope of 2,3-dihydrofurans.

S-Ethenylsulfoximine Derivatives. Reagents for Ethylenation of Protic Nucleophiles

Johnson, Carl R.,Lockard, James P.,Kennedy, Eugene R.

, p. 264 - 271 (2007/10/02)

The preparation of S-vinyl and S-(2-substituted)ethenyl derivatives of sulfoximines is described.Vinyl-, (2-phenylethenyl)-, (2,2-diphenylethenyl)-, (2-methyl-1-propenyl)-, (dimethylamino)phenyloxosulfonium fluoroborates were found to undergo an addition-elimination reaction sequence with protic nitrogen and carbon nucleophiles, resulting in ethylenation of the nucleophile and N,N-dimethylbenzenesulfinamide.Primary amines gave aziridines, enamines gave cyclopropyl derivatives of iminium salts or pyrrolidinium salts, anions of active methylene compounds gave dihydrofurans and/or cyclopropanes, and anions of nitroalkanes gave cyclic nitronic esters and/or nitrocyclopropanes.In several cases vinyl salts were generated in situ from β-methoxyoxosulfonium salts.Treatment of (-)-(S)-dimethylamino)phenyl(trans-2-phenylethenyl)oxosulfonium fluoroborate with methyl cyanoacetate in methanol containing sodium methoxide gave, in 81percent yield, (+)-(1S,2R)-methyl 1-cyano-2-phenylcyclopropanecarboxylate of 25.5percent optical purity.The same salt upon treatment with methyl nitroacetate gave, in 95percent yield, methyl 4-phenyl-3-isoxazolinecarboxylate 2-oxide with 33percent enantiomeric excess.Cyclopropanes were formed upon treatment of S-methyl-S-(trans-2-phenylethenyl)-N-(p-tolylsulfonyl)sulfoximine with anions of active methylene compounds.

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