86604-43-5

Usage

Uses

Used in Organic Synthesis:
2-[1-(3-Methoxy-phenyl)-ethylidene]-malononitrile is used as a key intermediate in the synthesis of complex organic molecules. Its unique structure allows for versatile reactions that can lead to the formation of a wide range of nitrogen-containing compounds, which are essential in various chemical processes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-[1-(3-Methoxy-phenyl)-ethylidene]-malononitrile serves as a valuable compound for the development of new drugs. Its chemical properties and reactivity make it a promising candidate for the creation of novel therapeutic agents, particularly those targeting specific biological pathways or mechanisms.
Used in Material Science:
2-[1-(3-METHOXY-PHENYL)-ETHYLIDENE]-MALONONITRILE's structural features also make it suitable for applications in material science. Its potential use in the development of new materials with unique properties, such as improved conductivity or enhanced stability, can contribute to advances in various technological fields.

InChI:InChI=1/C12H10N2O/c1-9(11(7-13)8-14)10-4-3-5-12(6-10)15-2/h3-6H,1-2H3

Upstream product

• 109-77-3 malononitrile 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 

Downstream Products

• 301847-64-3 1,1-di-(Methylthio)-3-(3-methoxyphenyl)-4,4-dicyano-butadiene 
• 1190415-65-6 2-amino-5,6,7,8-tetrahydro-4-(3-methoxyphenyl)-4,7,7-trimethyl-5-oxo-4H-benzo[b]pyran-3-carbonitrile 
• 1334740-50-9 (2E,4E)-2-cyano-6,6,6-trifluoro-3-(3-methoxyphenyl)-5-phenylhexa-2,4-dienamide 
• 1312594-20-9 2-bromo-6-methyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridin-4-amine 
• 1312594-19-6 4-amino-2-bromo-6-methyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridine-5-carboxylic acid 
• 1312594-18-5 ethyl 4-amino-2-bromo-6-methyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridine-5-carboxylate 
• 1312594-17-4 ethyl 4-amino-6-methyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridine-5-carboxylate 
• 86604-38-8 2-amino-4-[3-(methyloxy)phenyl]-3-thiophenecarbonitrile 
• 1312594-01-6 N-{4-{[(3-chlorophenyl)sulfonyl]amino}-6-methyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridin-2-yl}acetamide 
• 1312593-78-4 N-[6-methyl-3-[3-(methyloxy)phenyl]-2-(1H-pyrazol-4-yl)thieno[2,3-b]pyridin-4-yl]methanesulfonamide 
• 1312593-77-3 N-{2-bromo-6-methyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridin-4-yl}methanesulfonamide 
• 1312593-76-2 N-[6-methyl-3-[3-(methyloxy)phenyl]-2-(1H-pyrazol-4-yl)thieno[2,3-b]pyridin-4-yl]cyclopropanesulfonamide 
• 1312593-75-1 N-{2-bromo-6-methyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridin-4-yl}cyclopropanesulfonamide 
• 1312593-74-0 3-chloro-N-[6-methyl-3-[3-(methyloxy)phenyl]-2-(4-pyridinyl)thieno[2,3-b]pyridin-4-yl]benzenesulfonamide 

Relevant academic research and scientific papers

"on Water" Direct Catalytic Vinylogous Aldol Reaction of Silyl Glyoxylates

The unique reactivity of water in the direct catalytic vinylogous aldol reaction of silyl glyoxylates is reported. With the hydrogen-bonding networks from water, the unfavorable homogeneous reactions in organic solvents were severely suppressed, and the "

Phosphine-catalyzed domino reaction: A novel sequential [2+3] and [3+2] annulation reaction of γ-substituent allenoates to construct bicyclic[3, 3, 0]octene derivatives

We have successfully developed a novel and efficient phosphine-catalyzed sequential [2+3] and [3+2] annulation reaction of γ-substituent allenoates to construct bicyclic[3, 3, 0]octene derivatives. The protocol uses readily available γ-substituent allenoa

NOVEL COMPOUNDS

The present invention relates to novel NADPH oxidase II inhibitors and their use in the treatment of diseases mediated by the NADPH oxidase II enzyme.

Use of a solid hydrotalcite structure incorporating fluorides for basic catalysis of michael or knoevenagel reactions

The invention concerns the use of a solid basic catalyst comprising a hydrotalcite structure wherein part at least of the compensating anions are fluoride anions F? for producing Knoevenagel of Michael condensation reactions. The invention also concerns novel solid basic catalysts comprising a hydrotalcite structure characterised by a Mg/Al molar ratio ranging between 2.5 and 3.8 wherein at least part of the compensating anions are fluoride anions F?, and methods for preparing said novel catalysts.