14297-60-0

Basic information

• Product Name: 1,4-Benzenedicarboxylic acid, 2,5-bis(phenylamino)-, dimethyl ester
• CAS NO: 14297-60-0
• Molecular Formula: C22H20N2O4
• Molecular Weight: 376.412
• Mol File: 14297-60-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1,4-Benzenedicarboxylic acid, 2,5-bis(phenylamino)-, dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Benzenedicarboxylic acid, 2,5-bis(phenylamino)-, dimethyl ester(14297-60-0)
• EPA Substance Registry System: 1,4-Benzenedicarboxylic acid, 2,5-bis(phenylamino)-, dimethyl ester(14297-60-0)

Safety Data

• Hazardous Substances Data: 14297-60-0(Hazardous Substances Data)

Upstream product

• 27712-87-4 1,4-cyclohexanedione-2,5-di-carboxylic acid methyl ester 
• 62-53-3 aniline 
• 6289-46-9 dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate 
• 752-62-5 2.5-Bis--terephthalsaeure-dimethylester 
• 916-42-7 2.5-Bis--terephthalsaeure-dimethylester 
• 5870-37-1 2,5-Dihydroxybenzol-1,4-dicarbonsaeure-dimethylester 
• 865-15-6 2,5-Bis-<3,3-dibutyl-1-phenyl-ureido>-terephthalsaeure-dimethylester 
• 752-33-0 2,5-Bis-(3,3-diethyl-1-phenyl-ureido)-terephthalic acid dimethyl ester 
• 916-34-7 2,5-Bis-<3,3-dimethyl-1-phenyl-ureido>-terephthalsaeure-dimethylester 
• 4898-58-2 2,5-bis(phenylamino)-1,4-cyclohexadiene-1,4-dicarboxylic acid dimethyl ester 

Downstream Products

• 1047-16-1 Quinacridone 
• 369370-66-1 2,5-bis(diphenylamino)terephthaldicarboxaldehyde 
• 369370-61-6 dimethyl 2,5-bis(diphenylamino)terephthalate 
• 10109-95-2 2,5-di(phenylamino)-terephthalic acid 

Relevant articles and documents

Arylamine-Linked 2D Covalent Organic Frameworks for Efficient Pseudocapacitive Energy Storage

The development of new linkages is one of the most efficient strategies to enrich the diversity of covalent organic frameworks (COFs). Particularly, functional linkages can endow COFs with additional tailored properties besides the building units, which further diversify COFs with desirable functions. Herein, we have developed a new arylamine linkage for the construction of COFs. Two new arylamine-linked COFs (AAm-TPB and AAm-Py) were prepared by condensing cost-effective dimethyl succinyl succinate (DMSS) with corresponding multitopic amines (TPB-NH2 and Py-NH2). Due to the abundant electroactive diphenylamine moieties in the COF skeletons resembling that of polyaniline (PANI), a state-of-the-art conductive polymer, the pseudocapacitive energy storage performance of AAm-TPB was further investigated. Remarkably, the AAm-TPB electrode exhibits a high capacitance of 271 F g?1 with a three-electrode setup at a discharge rate of 1 A g?1, which represents one of the highest capacitances among the reported COF-based electrode materials.

Amplified spontaneous emission, optical waveguide and polarized emission based on 2,5-diaminoterephthalates

A series of 2,5-diaminoterephthalates with a simple structure were synthesized through one-step reaction, and their bar-shaped single crystals with a large size and a smooth surface have been obtained via the solvent-evaporation method. These crystals exh

Twisting strategy applied to N,N-diorganoquinacridones leads to organic chromophores exhibiting efficient solid-state fluorescence

A new molecular design of organic emitters exhibiting efficient solid-state fluorescence, which involves planarity breaking of N,N-diorganoquinacridones, is presented. The new design principle led to the development of dimethyl 2,5-diaminoterephthalates and 2,5-diamino-1,4-diaroylbenzenes, which emitted green to yellow and yellow to red light with high-to-excellent quantum yields, respectively. In addition, the photoluminescence properties of the diaroylbenzenes were dependent on the morphology and reversibly variable by thermal and solvent vapor stimuli.