19714-00-2

Upstream product

• 57697-64-0 mucochloric acid 
• 766-40-5 Mucochloric acid 

Downstream Products

• 117997-26-9 3,5-Dichloro-2-<5H>-furanon-4-yl di-O-ethyldithiophosphate 
• 142581-46-2 (3RS,4SR)-(+/-)-<(5RS)-3,4-Dichlor-2,5-dihydro-5-hydroxy-2-oxo-1H-pyrrol-1-yl>-1,4-diphenylazetidin-2-on 
• 142581-46-2 (3RS,4SR)-(+/-)-3-<(5SR)-3,4-Dichlor-2,5-dihydro-5-hydroxy-2-oxo-1H-pyrrol-1-yl>-1,4-diphenylazetidin-2-on 
• 28001-50-5 3,4-dichloro-5-hydroxy-1-phenyl-1,5-dihydropyrrol-2-one 
• 129256-37-7 4-anilino-3,5-dichlorofuran-2(5H)-one 
• 129256-40-2 4,5-bis(phenylamino)-3-chlor-5(H)-furan-2-on 
• 129256-41-3 3,5-Bis(phenylamino)-4-chlor-1-phenyl-3-pyrrolin-2-on 
• 1252934-65-8 5-(2-aminophenylamino )-3,4-dichlorofuran-2(5H)-one 
• 106435-53-4 2-chloromethyl-quinoxaline 
• 28001-51-6 α,β-dichloro-?-hydroxy-N-benzylcrotonic lactam 

Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR VIRAL SENSITIZATION

Provided are compounds that enhance the efficacy of viruses by increasing spread of the virus in cells, increasing the titer of virus in cells, or increasing the antigen expression from a virus, gene or trans-gene expression from a virus, or virus protein expression in cells. Other uses, compositions and methods of using same are also provided.

A new synthesis of novel tricyclic 2(5H)-furanone heterocycles from 3,4,5-trichloro-2(5H)-furanone

A novel class of five-six-six tricyclic 2(5H)-furanone heterocycles was synthesized from 3,4,5-trichloro-2(5H)-furanone and bifunctional o-nucleophiles in a single step. In addition, 2-(chloromethyl)quinoxaline was obtained through this method, and the distinctive formation mechanism of this compound is discussed.

NOVEL 4-AMINO-2(5H)-FURANONES

The present invention relates to compounds of formula (I): wherein X is selected from hydrogen, a halogen, a substituted or unsubstituted cyclic and heterocyclic moiety, substituted or unsubstituted, linear or branched alkyl, alkyloxy, alkylcarbonyl, alky