924906-47-8

Basic information

• Product Name: 2-benzyl-5-ethylidene-6-oxo-4-vinyl-1,2,5,6-tetrahydropyridine-2-carboxylic acid methyl ester
• Synonyms: 2-benzyl-5-ethylidene-6-oxo-4-vinyl-1,2,5,6-tetrahydropyridine-2-carboxylic acid methyl ester
• CAS NO: 924906-47-8
• Molecular Weight: 297.354
• Mol File: 924906-47-8.mol

Chemical Properties

• CAS DataBase Reference: 2-benzyl-5-ethylidene-6-oxo-4-vinyl-1,2,5,6-tetrahydropyridine-2-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-5-ethylidene-6-oxo-4-vinyl-1,2,5,6-tetrahydropyridine-2-carboxylic acid methyl ester(924906-47-8)
• EPA Substance Registry System: 2-benzyl-5-ethylidene-6-oxo-4-vinyl-1,2,5,6-tetrahydropyridine-2-carboxylic acid methyl ester(924906-47-8)

Safety Data

• Hazardous Substances Data: 924906-47-8(Hazardous Substances Data)

Upstream product

• 924906-70-7 methyl 2-benzyl-2-(1-oxo-but-2-ynylamino)hexa-3,4-dienoate 

Downstream Products

• 933996-07-7 (8a-benzyl-6-ethylidene-3,5-dioxo-7-vinyl-6,8a-dihydro-5H-oxazolo[3,4-a]pyridin-1-ylideneamino)-acetic acid methyl ester 
• 933996-04-4 [(2-benzyl-5-ethylidene-6-oxo-4-vinyl-1,2,5,6-tetrahydro-pyridine-2-carbonyl)-amino]-acetic acid methyl ester 
• 933996-08-8 8a-benzyl-6-ethylidene-1-isobutylimino-7-vinyl-6,8a-dihydro-1H-oxazolo[3,4-a]pyridine-3,5-dione 
• 933996-05-5 2-benzyl-5-ethylidene-6-oxo-4-vinyl-1,2,5,6-tetrahydro-pyridine-2-carboxylic acid isobutyl-amide 

Relevant articles and documents

Rhodium(I)-catalyzed allenic carbocyclization reaction affording δ- and ε-lactams

(Chemical Equation Presented) This letter extends the scope of the rhodium(I)-catalyzed allenic Alder-ene carbocyclization reaction to the preparation of δ- and ε-lactams from amides. A variety of allenic propiolamides were cycloisomerized to give a numbe

Cycloaddition reactions of amino-acid derived cross-conjugated trienes: Stereoselective synthesis of novel heterocyclic scaffolds

Cross-conjugated trienes obtained via a Rh(I)-catalyzed allenic Alder-ene reaction represent a new class of compounds. The synthesis of heterocyclic compounds containing multiple fused rings was accomplished via sequential Diels-Alder reactions of amino-a