19883-35-3

Basic information

• Product Name: (Z)-N-(2-phenylethenyl)-2-pyrrolidinone
• Synonyms: (Z)-N-(2-phenylethenyl)-2-pyrrolidinone
• CAS NO: 19883-35-3
• Molecular Weight: 187.241
• Mol File: 19883-35-3.mol
• Article Data: 25

Chemical Properties

• CAS DataBase Reference: (Z)-N-(2-phenylethenyl)-2-pyrrolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-N-(2-phenylethenyl)-2-pyrrolidinone(19883-35-3)
• EPA Substance Registry System: (Z)-N-(2-phenylethenyl)-2-pyrrolidinone(19883-35-3)

Safety Data

• Hazardous Substances Data: 19883-35-3(Hazardous Substances Data)

Upstream product

• 616-45-5 2-pyrrolidinon 
• 122-78-1 phenylacetaldehyde 
• 13909-34-7 N-benzylidenephenylsulfonamide 
• 53934-76-2 N-(2-pyrrolidone)-2-acetic acid 
• 96-09-3 styrene oxide 
• 10147-11-2 propargyl benzene 
• 88-12-0 1-ethenyl-2-pyrrolidinone 
• 108-86-1 bromobenzene 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 31282-95-8 1-(chloromethyl)pyrrolidin-2-one 
• 189809-02-7 1-(tosylmethyl)-2-pyrrolidinone 
• 100-39-0 benzyl bromide 
• 108-90-7 chlorobenzene 
• 536-74-3 phenylacetylene 

Downstream Products

• 10135-23-6 N-(2-phenylethyl)pyrrolidin-2-one 
• 1174295-40-9 3,3′-(2-phenylethane-1,1-diyl)bis(1H-indole) 
• 1449753-76-7 C₂₅H₂₃Cl₂NO 
• 1449753-71-2 (Z)-1-(1,2-diphenylvinyl)pyrrolidin-2-one 
• 1609649-51-5 1-[2-phenyl-(1-phenylthio)ethyl]-2-pyrrolidinone 
• 1329422-45-8 (Z)-1-(2-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)pyrrolidin-2-one 

Relevant articles and documents

Iridium-Catalyzed β-C(sp2)?H Borylation of Enamides – Access to 3,3-Dihalogeno-2-methoxypiperidines

An efficient catalytic preparation of synthetically useful new β-borylated enamides was achieved under relatively mild conditions via a regioselective iridium-catalyzed C(sp2)?H borylation. The method features broad substrate scope, good functi

Anti-Markovnikov stereoselective hydroamination and hydrothiolation of (hetero)aromatic alkynes using a metal-free cyclic trimeric phosphazene base

Hydroamination and hydrothiolation are the most efficient and completely atom-economical process to construct important enamine and vinyl sulfide intermediates in pharmaceutical and organic chemistry. The cyclic trimeric phosphazene base (CTPB) showed gre

Regioselective hydrothiolation of alkenes bearing heteroatoms with thiols catalyzed by palladium diacetate

In sharp contrast to many examples of transition-metal-catalyzed hydrothiolation of alkynes, the corresponding catalytic addition of thiols to alkenes has remained undeveloped. However, a novel Pd-catalyzed addition of thiols to alkenes bearing a heteroatom, such as oxygen and nitrogen, is found to proceed under mild conditions to give the corresponding Markovnikov adducts, regioselectively, in good yields.