899-25-2

Upstream product

• 122-39-4 diphenylamine 
• 122-04-3 4-nitro-benzoyl chloride 

Downstream Products

• 87200-34-8 3--2-oxobenzoxazole 
• 87200-37-1 3--2-thiobenzoxazole 
• 126479-66-1 N,N-Diphenyl-4-{[1-(2-p-tolyl-1H-indol-3-yl)-meth-(Z)-ylidene]-amino}-benzamide 
• 87200-27-9 4-(2-nitro-3,4-dimethoxybenzylidene)amino-N,N-diphenylbenzamide 
• 126479-67-2 4-{[1-[2-(4-Chloro-phenyl)-1H-indol-3-yl]-meth-(Z)-ylidene]-amino}-N,N-diphenyl-benzamide 
• 126479-68-3 4-{[1-[2-(4-Methoxy-phenyl)-1H-indol-3-yl]-meth-(Z)-ylidene]-amino}-N,N-diphenyl-benzamide 
• 126479-65-0 N,N-Diphenyl-4-{[1-(2-phenyl-1H-indol-3-yl)-meth-(Z)-ylidene]-amino}-benzamide 
• 87200-35-9 3--6-nitro-2-oxobenzoxazole 
• 87200-31-5 1--3-(p-tolyl)thiourea 
• 87200-24-6 4-(p-methoxybenzylidene)amino-N,N-diphenylbenzamide 
• 87200-26-8 4-(3,4-dimethoxybenzylidene)amino-N,N-diphenylbenzamide 
• 87200-23-5 4-(o-methoxybenzylidene)amino-N,N-diphenylbenzamide 
• 87200-33-7 1--3-(p-bromophenyl)thiourea 
• 126479-83-2 4-{3-(2-Chloro-phenoxy)-2-[2-(4-methoxy-phenyl)-1H-indol-3-yl]-4-oxo-azetidin-1-yl}-N,N-diphenyl-benzamide 

Relevant academic research and scientific papers

A novel ultrasound-sensitive mechanofluorochromic AIE-compound with remarkable blue-shifting and enhanced emission

A novel ultrasonic-sensitive mechanofluorochromic AIE-compound (ITPADA) has been designed and synthesized. The fluorescent properties of the ITPADA suspensions were greatly affected by the ultrasonic treatment and extremely sensitive to its power, which s

Imide-containing aromatic diamine compound of the structure and its preparation method and application

The invention discloses an aromatic diamine compound containing an imide structure as well as a preparation method and application thereof. The method for preparing the aromatic diamine compound containing the imide structure comprises the following steps of: preparing a rigid non-planar distorted structural intermediate containing the imide structure by high reaction activity of acyl chloride and active hydrogen; introducing different chemical groups through the Suzuki reaction of halogen elements and boric acid ester; utilizing fluoronitrobenzene to react with amino so as to preparing a binitro product by reaction of fluoronitrobenzene and amino; and reducing to obtain a novel aromatic diamine compound containing the imide structure. The synthesizing method is simple, easy to purify and high in yield; the synthesized compound has unique fluorescent characteristic, excellent thermal property and solubility property, can be used as a photoelectric material and a monomer for synthesizing novel high-performance polymers such as polyamide, polyimide, polyamide imide and polyester imide.

Synthesis and CNS Activity of 4-Arylideneamino-N,N-diphenylbenzamides, 1--3-(p-substituted phenyl)thioureas and 6-Substituted 3-2-oxo/thio-benzoxazoles

4-Arylideneamino-N,N-diphenylbenzamides (IIIa-h), 1--3-(p-substituted phenyl)thioureas (IVa-d) and 6-substituted 3--2-oxo-/thio-benzoxazoles (Va-d) have been synthesized from 4-amino-N,N-diphenylbenzamide (IIa).Similarly thioureas IVe-h and benzoxazoles Ve-h have been prepared from 2-aminoquinazolin-4(3H)-one (IIb).Compounds III, IV and V are found to be psychotropic and nontoxic.