115411-35-3

Upstream product

• 98-86-2 acetophenone 
• 19607-08-0 methyl 2-methoxycarbonyl-3,3-di(methylsulfanyl)acrylate 

Downstream Products

• 114361-54-5 4-methylsulfanyl-6-phenyl-2-oxo-1,2-dihydropyridine 
• 2128-90-7 6-phenyl-2H-pyran-2-one 
• 5526-38-5 4-hydroxy-6-phenyl-2H-pyran-2-one 
• 115411-59-1 4-methoxy-6-(p-methoxyphenyl)-2H-pyran-2-one 
• 115411-39-7 methyl 4-hydroxy-2-oxo-6-phenyl-2H-pyran-3-carboxylate 
• 115411-40-0 methyl 4-methoxy-6-phenyl-2-oxo-2H-pyran-3-carboxylate 
• 115411-42-2 2-phenylpyrano<3,4-d>pyrido<1,2-a>pyrimidine-4,5(4H,5H)-dione 
• 115411-68-2 methyl 4-methoxy-6-(p-methoxyphenyl)-2-oxo-2H-pyran-3-carboxylate 
• 115411-41-1 methyl 4-anilino-2-oxo-6-phenyl-2H-pyran-3-carboxylate 
• 115411-43-3 dimethyl 3-methoxycarbonyl-2-oxo-6-phenyl-2H-pyran-4-ylmalonate 
• 1214890-94-4 C₁₇H₁₈O₆S 
• 1448898-25-6 methyl 8-(methylthio)-2,6-diphenyl-4,5-dihydro-2H-benzo[e]indazole-9-carboxylate 
• 1448900-75-1 (Z)-methyl 2-(6-chloro-7-hydroxy-4-phenyl-2H-chromen-2-ylidene)acetate 

Relevant academic research and scientific papers

Transition metal-free synthesis of sterically hindered allylarenes from 5-hexene-2-one

A simple, efficient and transition metal-free strategy was established for the synthesis of highly functionalized, sterically hindered allylarenes (6, 7 & 8) by base-mediated ring transformation of 2-oxo-6-aryl-4-(methylthio/sec-amino)-2H-pyran-3-carbonit

Thieno[3,2-: C] pyran: An ESIPT based fluorescence "turn-on" molecular chemosensor with AIE properties for the selective recognition of Zn2+ion

Excited state intramolecular proton transfer (ESIPT) based functionalized thieno[3,2-c]pyran P was designed and synthesized as a fluorescent turn-on chemosensor for the selective recognition of Zn2+ ion with a low detection limit (0.67 μM). Fourier transf

Synthesis of substituted 2H-benzo[e]indazole-9-carboxylate as a potent antihyperglycemic agent that may act through IRS-1, Akt and GSK-3β pathways

Based on high throughput screening of our chemical library, we identified two 4,5-dihydro-2H-benzo[e]indazole derivatives (5d and 5g), which displayed a significant effect on glucose uptake in L6 skeletal muscle cells. Based on these lead molecules, a ser

Synthesis, electrochemical and optical properties of stable yellow fluorescent fluoranthenes

Figure presented A novel series of thermally stable yellow light emitting fluoranthenes with an amine donor and a nitrile acceptor was prepared from a ketene-S,S-acetal under mild conditions without using an organometal catalyst. The organic light emitting device of yellow fluoranthene 10b exhibited substantially low turn-on voltage (2.6 V) and maximum brightness of 470 Cd/m2 with luminance efficiency of 2.0 Cd/A without using any dopant.

Reaction of 6-aryl- or styryl-4-methylsulfanyl-2-oxo-2H-pyrans with active methylene compounds and fluorescence properties of the products

(Chemical Equation Presented)New 2-pyrone derivatives, dialkyl 3-cyano-6-phenyl-2-oxo-2H-pyran-4-ylmalonates and alkyl 3-cyano-6-phenyl-2-oxo- 2H-pyran-4-ylacetates, which were easily prepared by the reaction of 6-aryl-4-methyl-sulfanyl-2-oxo-2H-pyran-3-c

Synthesis and fluorescence of 2H-pyrone derivatives for organic light-emitting diodes (OLED)

(Chemical Equation Presented) 2H-Pyrone derivatives were synthesized through the reaction of aryl acetyl compounds with ketene dithioacetals in the presence of sodium hydroxide, and they showed very strong fluorescence in the solid state. The light-emitti

Substituent directed regioselective synthesis of 2-oxonicotonic acids and methyl nicotinates

An innovative synthesis of aryl tethered 1,2-dihydro-2-oxopyridine-3-carboxylic acids has been developed through nucleophile induced ring transformation of methyl 6-aryl-4-methylsulfanyl-2H-pyran-2-one-3-carboxylates using either cyanamide or arylamidine

Synthesis of arylated highly congested indans using a domino sequence

A novel and efficient regioselective synthesis of various arylated highly congested 7-aryl-5-methylsulfanylindan-4-carbonitriles (3a-f), methyl 7-aryl-5-methylsulfanylindan-4-carboxylates (10a-e) and 7-aryl-5-methylsulfanylindan-4-carboxylic acids (11a-e)

Acetyltrimethylsilane: A novel reagent for the transformation of 2H-pyran-2-ones to unsymmetrical biaryls

An expeditious synthesis of unsymmetrical biaryls functionalized with electron-withdrawing or -donating substituents is described and illustrated by carbanion-induced ring transformation of 2H-pyran-2-one using acetyltrimethylsilane (ATMS) as a novel reag

A vicarious synthesis of unsymmetrical meta- and para- terphenyls from 2H-pyran-2-ones

An innovative synthesis of terphenyls functionalized with electron-withdrawing or -donating substituents is described and illustrated by carbanion-induced ring transformation of 2H-pyran-2-ones with 2-methoxyacetophenone in excellent yields. The existing