56419-89-7

Basic information

• Product Name: N-Benzanilide-4,4'-dicarboxylic acid
• Synonyms: 4,4'-(Carbonylimino)dibenzoic acid;4-[(4-Carboxybenzoyl)amino]benzoic acid;N-Benzanilide-4,4'-dicarboxylic acid
• CAS NO: 56419-89-7
• Molecular Formula: C₁₅H₁₁NO₅
• Molecular Weight: 285.25154
• Mol File: 56419-89-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: >330 °C
• Boiling Point: 463.6±30.0 °C(Predicted)
• Appearance: /
• Density: 1.475
• PKA: 3.80±0.10(Predicted)
• CAS DataBase Reference: N-Benzanilide-4,4'-dicarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzanilide-4,4'-dicarboxylic acid(56419-89-7)
• EPA Substance Registry System: N-Benzanilide-4,4'-dicarboxylic acid(56419-89-7)

Safety Data

• Hazardous Substances Data: 56419-89-7(Hazardous Substances Data)

Usage

General Description

N-Benzanilide-4,4'-dicarboxylic acid is a chemical compound containing an N-benzanilide group and two carboxylic acid groups. It is commonly used in the synthesis of various pharmaceuticals and organic compounds. N-Benzanilide-4,4'-dicarboxylic acid has been studied for its potential as an antitumor agent and for its ability to inhibit certain enzymes. It also has potential applications in the development of new materials with specific properties, such as liquid crystals. Overall, N-Benzanilide-4,4'-dicarboxylic acid is a versatile compound with a range of potential uses in the field of chemistry and materials science.

Upstream product

• 6876-66-0 4,4'-dimethylbenzanilide 
• 7377-26-6 4-Methoxycarbonylbenzoyl chloride 
• 619-45-4 4-methoxycarbonyl aniline 
• 150-13-0 4-amino-benzoic acid 
• 100-20-9 terephthaloyl chloride 
• 18708-46-8 terephthaloyl chloride 

Downstream Products

• 1431562-76-3 Cd(4,4′-(carbonylimino)dibenzoato)(H2O) 
• 1431562-77-4 Zn(4,4′-(carbonylimino)dibenzoato)(H2O) 
• 1429917-67-8 [Zn(4,4′-(carbonylimino)dibenzoato)(4,4′-bipyridine)]·DMF*H₂O 

Relevant articles and documents

Syntheses, Structures and Sorption Properties of Three Isoreticular Trinuclear Indium-Based Amide-Functionalized Metal–Organic Frameworks

Amide-functionalized metal–organic frameworks (AFMOFs) as a subclass of MOF materials have received great interest recently because of their intriguing structures and diverse potential applications. In this work, solvothermal reactions between indium nitrate and two mixed-linkers afforded two new isoreticular 8-connected trinuclear indium-based AFMOFs of [(In3O)(OH)(L2)2(IN)2]?(solv)x (2-In) and [(In3O)(OH)(L2)2(AIN)2]?(solv)x (NH2-2-In) (H2L2=4,4′-(carbonylimino)dibenzoic acid and HIN=isonicotinic acid or HAIN=3-aminoisonicotinic acid), respectively. Moreover, by means of reticular chemistry, an extended network of [(In3O)(OH)(L3)2(PB)2]?(solv)x (3-In) (H2L3=4,4′-(terephthaloylbis(azanediyl))dibenzoic acid, HPB=4-(4-pyridyl)benzoic acid) was also successfully realized after prolongation of the former dicarboxylate linker and HIN, resulting in a truly 8-connected isoreticular AFMOF platform. These frameworks were structurally determined by single-crystal X-ray diffraction (SCXRD). Sorption studies further demonstrate that 2-In and NH2-2-In exhibit not only high surface areas and pore volumes but also relatively high carbon capture capabilities (the CO2 uptakes reach 60.0 and 75.5 cm3 g?1 at 298 K and 760 torr, respectively) due to the presences of amide and/or amine functional groups. The selectivity of CO2/N2 and CO2/CH4 calculated by IAST are 10.18 and 12.43, 4.20 and 4.23 for 2-In and NH2-2-In, respectively, which were additionally evaluated by mixed-gases dynamic breakthrough experiments. In addition, high-pressure gas sorption measurements show that both materials could take up moderate amounts of natural gas.

SULFURIC ACID ESTERS OF SUGAR ALCOHOLS

The present invention is concerned with novel sulfuric acid esters of sugar alcohols and sugar alcohol-like compounds of the formula STR1 Also described are methods for the treatment and/or prophylaxis of arteriosclerotic changes in the vascular wall as well as a process for the manufacture of the compounds of formula I and their salts.

Mesogenic glycidyl esters

Glycidyl esters are disclosed which contain mesogenic moieties which result in improved properties when cured.