134161-81-2

Basic information

• Product Name: 2H-Pyran-3-carbonitrile, 6-(4-methylphenyl)-4-(methylthio)-2-oxo-
• CAS NO: 134161-81-2
• Molecular Formula: C14H11NO2S
• Molecular Weight: 257.313
• Mol File: 134161-81-2.mol
• Article Data: 31

Chemical Properties

• CAS DataBase Reference: 2H-Pyran-3-carbonitrile, 6-(4-methylphenyl)-4-(methylthio)-2-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran-3-carbonitrile, 6-(4-methylphenyl)-4-(methylthio)-2-oxo-(134161-81-2)
• EPA Substance Registry System: 2H-Pyran-3-carbonitrile, 6-(4-methylphenyl)-4-(methylthio)-2-oxo-(134161-81-2)

Safety Data

• Hazardous Substances Data: 134161-81-2(Hazardous Substances Data)

Upstream product

• 3490-92-4 methyl 2-cyano-3,3-bis(methylsulfanyl)acrylate 
• 122-00-9 para-methylacetophenone 
• 585-74-0 3-Methylacetophenone 
• 104-87-0 4-methyl-benzaldehyde 
• 17823-58-4 ethyl 2-cyano-3,3-di(methylsulfanyl)acrylate 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 136358-75-3 5-(cyanomethyl)-1-methyl-3-(4-methylphenyl)pyrazole 
• 136358-70-8 3-(cyanomethyl)-1-methyl-5-(4-methylphenyl)pyrazole 
• 147503-06-8 2-(3-(p-tolyl)isoxazol-5-yl)acetonitrile 
• 57663-07-7 4-methylsulfanyl-2-oxo-6-p-tolyl-1,2-dihydro-pyridine-3-carbonitrile 
• 1206525-10-1 C₂₃H₁₉NO₂ 
• 1415327-68-2 [2-(4-methylphenyl)-4H-benzo[d]pyrimido[2,1-b][1,3]thiazol-4-yliden]acetonitrile 
• 1415327-69-3 [8-methoxy-2-(4-methylphenyl)-4Hbenzo[d]pyrimido[2,1-b][1,3]thiazol-4-yliden]acetonitrile 
• 1417815-64-5 (2E)-2-((2-phenyl)-3-(pyridin-2-yl)-6-p-tolylpyrimidin-4(3H)-ylidene)acetonitrile 
• 1417815-73-6 (2E)-2-(2-(4-chlorophenyl)-3-(pyridin-2-yl)-6-p-tolylpyrimidin-4(3H)-ylidene)acetonitrile 
• 1417815-77-0 (2E)-2-(2-(3-chlorophenyl)-3-(pyridin-2-yl)-6-p-tolylpyrimidin-4(3H)-ylidene)acetonitrile 
• 1434247-24-1 1-(4-methylphenyl)-3-(methylthio)-5H-dibenzo[d,f][1,3]diazepin-6(7H)-one 

Relevant articles and documents

Synthesis of Solution-Processable Donor-Acceptor Pyranone Dyads for White Organic Light-Emitting Devices

A series of donor-acceptor pyranones (3a-m, 4a-h) were synthesized using α-oxo-ketene-S,S-acetal as the synthon for their application as emissive materials for energy-saving organic light-emitting devices (OLEDs). Among them, five pyranones 3f, 3g, 3h, 3m

Synthesis, spectral characterization and photophysical studies of tetrahydroquinolines

A metal-free, ultrasound-assisted, fast synthesis of fluorescent N-Boc-protected 1,2,3,4–tetrahydroquinolines 9a-p is described through carbanion-induced ring transformation of 6-aryl-2H-pyran-2-ones 7 with tert?butyl 3-oxopiperidine-1-carboxylate 8 under

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