35977-95-8

Upstream product

• 614-16-4 Benzoylacetonitrile 
• 1823-99-0 3-amino-3-phenylacrylonitrile 

Downstream Products

• 35978-00-8 5-oxo-1-phenyl-5H-thiazolo[3,2-a]quinazoline-2-carbonitrile 
• 35978-05-3 7-methyl-5-oxo-1-phenyl-5H-thiazolo[3,2-a]quinazoline-2-carbonitrile 
• 13053-82-2 N-(1,3-thiazol-2-yl)benzamide 
• 3161-35-1 3-Oxo-3-phenyl-2-[4-phenyl-[1,3]dithiol-(2Z)-ylidene]-propionitrile 
• 40816-01-1 1.5-Diphenyl-4-cyan-epidithio-Δ^1.3-pentadienon-(5) 
• 138990-89-3 3-Oxo-3-phenyl-2-[4-phenyl-[1,2]dithiol-(3Z)-ylidene]-propionitrile 
• 1146597-08-1 4,4'-(1,3-phenylene)bis(2,6-diphenyl-5-(trifluoromethyl)nicotinonitrile) 
• 1146597-17-2 4,4'-(1,2-phenylene)bis(2-(4-tert-butylphenyl)-6-phenylpyridine-3,5-dicarbonitrile) 
• 1146597-13-8 4,4'-(1,2-phenylene)bis(6-(biphenyl-4-yl)-2-phenylnicotinonitrile) 
• 1146596-99-7 4,4'-(1,4-phenylene)bis(2-phenyl-6-p-tolylpyridine-3,5-dicarbonitrile) 
• 1146597-05-8 4,4'-(1,3-phenylene)bis(2-phenyl-6-p-tolylnicotinonitrile) 
• 1146596-95-3 4,4'-(1,4-phenylene)bis(2-phenyl-6-p-tolylnicotinonitrile) 
• 704870-71-3 2-amino-4-phenylthiazole-5-carbonitrile 
• 31879-47-7 2-benzoyl-3-oxo-3-phenylpropanenitrile 

Relevant academic research and scientific papers

Tetrabromo hydrogenated cardanol: Efficient and renewable brominating agent

(Chemical Equation Presented) 2,4,4,6-Tetrabromo-3-n-pentadecyl-2,5- cyclohexadienone (TBPCO) has been synthesized and used as a new efficient, convenient, and environmentally friendly brominating agent.

2-ACYLAMINOTHIAZOLE DERIVATIVES

The Invention relates to compounds of the formula I, wherein the variables are as defined in the claims, for use as a medicament. The compounds are A2A-receptor legends and are useful in the treatment of neurological and psychiatric disorders where an A2A-receptor is implicated.

Electrochemical synthesis of 5-amino-4-benzoyl-3-phenylfuran-2- carbonitrile

Cathodic reduction of 2-bromo-2-cyanoacetophenone afforded 5-amino-4- benzoyl-3-phenylfuran-2-carbonitrile in an one pot reaction. The process is discussed and all the secondary products are isolated and characterized.

1-(DITHIOLYLIDENE)-1-CYANOACETOPHENONES FROM DITHIOLETHIONE-BROMINE ADDUCTS WITH ENAMINONITRILES

Title compounds are easily prepared by reaction of dithiolethione-bromine adducts with enaminonitriles followed by treatment with triethylamine.The mechanism that accounts for their formation is discussed. Key Words: 1,2-Dithiole-3-thiones; 1,3-dithiole-2-thiones; 1-(1,2-dithiol-3-ylidene)-1-cyanoacetophenones; 1-(1,3-dithiol-2-ylidene)-1-cyanoacetophenones; 3-amino-3-arylpropenenitriles.

A CONVENIENT SYNTHESIS OF 2-ALKYL- and 2-ARYLAMINO-4-ARYL-5-CYANOTHIAZOLES

The reactions of a series of para-substituted 3-amino-3-aryl-propenenitriles 1a-f with N-phenyl- (2a) and N-methyl-S-chloroisothiocarbamoyl chloride (2b), followed by triethylamine treatment, provide 2-phenyl- and 2-methyl-4-aryl-5-cyanothiazoles 3a-i.N-M