704914-80-7

Basic information

• Product Name: 4-(bis(4-Methoxyphenyl)aMino)benzoic acid
• Synonyms: 4-(bis(4-Methoxyphenyl)aMino)benzoic acid;1-(4-(bis(4-Methoxyphenyl)aMino)phenyl)ethanone
• CAS NO: 704914-80-7
• Molecular Formula: C₂₁H₁₉NO₄
• Molecular Weight: 349.37986
• Mol File: 704914-80-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 550.0±45.0 °C(Predicted)
• Appearance: /
• Density: 1.242±0.06 g/cm3(Predicted)
• PKA: 4.55±0.10(Predicted)
• CAS DataBase Reference: 4-(bis(4-Methoxyphenyl)aMino)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(bis(4-Methoxyphenyl)aMino)benzoic acid(704914-80-7)
• EPA Substance Registry System: 4-(bis(4-Methoxyphenyl)aMino)benzoic acid(704914-80-7)

Safety Data

• Hazardous Substances Data: 704914-80-7(Hazardous Substances Data)

Usage

General Description

4-(bis(4-Methoxyphenyl)aMino)benzoic acid is a chemical compound with the formula C21H20N2O4. It belongs to the class of compounds known as benzoic acids and derivatives, which are organic compounds containing a benzene ring which bear at least one carboxyl group. 4-(bis(4-Methoxyphenyl)aMino)benzoic acid is used in the field of organic chemistry as a building block for the synthesis of various pharmaceuticals and agrochemicals. It also exhibits potential pharmacological properties, making it a subject of interest for medicinal chemistry research. Additionally, it is employed in the production of dyes and pigments, and is used as a pH indicator in analytical chemistry.

Upstream product

• 696-62-8 para-iodoanisole 
• 619-45-4 4-methoxycarbonyl aniline 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 101-70-2 bis(4-methoxyphenyl)amine 
• 619-44-3 methyl 4-iodobenzoate 
• 704914-79-4 C₂₂H₂₁NO₄ 

Downstream Products

• 944474-16-2 N-(4-(1H-benzimidazol-2-yl)phenyl)-N,N-bis(4-methoxyphenyl)amine 
• 913614-33-2 C₄₂H₃₃N₅O₃ 

Relevant articles and documents

Triarylamine Enriched Organostannoxane Drums: Synthesis, Optoelectrochemical Properties, Association Studies, and Gelation Behavior

The straightforward synthesis of three organotin clusters endowed with six triarylamine-based moieties is reported herein. The optoelectronic properties of the molecules, as well as their ability to form gels, were investigated. The association ability of the compounds was studied as well by means of variable temperature nuclear magnetic resonance (NMR) and ultraviolet-visible (UV-vis) spectroscopy. The optimization of the geometry of the compounds has been performed and compared to the X-ray diffraction of the crystals. The results obtained through this comparison are useful for the explanation of their different gelation behaviors. In fact, organostannoxane drum 1 exhibits a strong ability to form organized supramolecular structures by means of a number of noncovalent short contacts that finally yield luminescent organogels in aromatic solvents.

Synthesis- and oxidation of triarylamine derivatives bearing hydrogen-bonding groups

(Chemical Equation Presented) Hydrogen-bonding triarylamines, 4-(N,N-bis(4-medioxyphenyl)amino)benzoic acid (TPA1), 5-(N,N-bis(4- methoxyphenyl)amino)isophthalic acid (TPA2), and N-(4-(1H-benz-imidazol-2-yl) phenyl)-N,N-bis(4-methoxyphenyl)amine (BImTPA),