18510-93-5

Usage

Physical state

White to off-white crystalline solid

Solubility

Sparingly soluble in water, soluble in organic solvents

Usage

Reagent for the detection and determination of aldehydes and ketones in chemical reactions
Building block for the synthesis of pharmaceuticals, agrochemicals, and dyes
Precursor in the production of other organic compounds
Reagent in various organic transformations
Wide range of applications in research and development of new chemical compounds
Used in the field of organic chemistry.

Upstream product

• 842-74-0 4-benzylidene-2-phenyloxazole-5(4H)-one 
• 100-63-0 phenylhydrazine 
• 18510-92-4 N-hydroxy-3,N-diphenyl-2-thiobenzoylamino-acrylamide 
• 16446-30-3 4-benzylidene-2-phenyl-4H-thiazol-5-one 
• 17606-70-1 (4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one 

Downstream Products

• 126933-98-0 2,3-Diphenyl-5-[1-phenyl-meth-(Z)-ylidene]-1,2,4-triaza-bicyclo[4.2.0]octa-3,6-dien-8-one 
• 126933-92-4 1-Acetyl-2,3-diphenyl-5-[1-phenyl-meth-(Z)-ylidene]-2,5-dihydro-1H-[1,2,4]triazin-6-one 
• 126934-09-6 8-benzylidene-8,8a-dihydro-8a-hydroxy-3-methyl-5,6-diphenyl-5H-1,2,4-oxadiazolo<5,4-f><1,2,4>triazine 
• 126934-01-8 2,3,7-Triphenyl-5-[1-phenyl-meth-(Z)-ylidene]-1,2,4-triaza-bicyclo[4.2.0]octa-3,6-dien-8-one 
• 126933-95-7 2,3-Diphenyl-1-phenylacetyl-5-[1-phenyl-meth-(Z)-ylidene]-2,5-dihydro-1H-[1,2,4]triazin-6-one 
• 126934-05-2 3-Benzyl-5,6-diphenyl-8-[1-phenyl-meth-(Z)-ylidene]-5,8-dihydro-[1,2,4]triazolo[3,4-f][1,2,4]triazine 
• 126934-08-5 8-benzylidene-1,4,8,8a-tetrahydro-8a-hydroxy-3-methyl-5,6-diphenyl-s-triazolo<3,4-f><1,2,4>triazine 
• 126934-10-9 3-Benzyl-5,6-diphenyl-8-[1-phenyl-meth-(Z)-ylidene]-5,8-dihydro-[1,2,4]oxadiazolo[5,4-f][1,2,4]triazin-8a-ol 
• 126934-06-3 3-Benzyl-1,5,6-triphenyl-8-[1-phenyl-meth-(Z)-ylidene]-5,8-dihydro-1H-[1,2,4]triazolo[3,4-f][1,2,4]triazin-8a-ol 
• 126953-67-1 2,3-Diphenyl-5-[1-phenyl-meth-(Z)-ylidene]-2,5-dihydro-1H-[1,2,4]triazin-6-one 

Relevant academic research and scientific papers

Synthesis and reactions of imidazolinones and triazolotriazines

4-Arylidene-2-phenyl-2-imidazoline-5-thiones (2) react with alkyl halides and ethyl chloroacetate in EtONa to give alkylthioimidazoles (3).The chalcones (5) obtained from the reaction of 4-arylidene-2-phenyl-1-(p-phenacetyl)-2-imidazolin-5-ones (4) and ar

Hydrazinolysis of Unsaturated Azlactones and Cyclisation of the Acrylic Acid Hydrazides into Tetrahydrotriazine, Pyrazolidine and Imidazoline Derivatives

Hydrazinolysis of 4-arylmethylene-2-oxazolin-5-ones (1) gives the corresponding acrylic acid hydrazides (5) among which the N-substituted hydrazides (5; R2=H) afford 5-aryl-methylene-3-phenyl-1,2,5,6-tetrahydro-1,2,4-triazin-6-ones (8) on heating with aq. sodium hydroxide and with excess of hydrazine hydrate, respectively.However, the N-phenylhydrazides (5; R2=Ph) give the corresponding 1-anilinio-4-arylmethylene-2-phenyl-2-imidazolin-5-ones (9) by simple heating.All steps can be carried out in the same flask.