747-06-8

Usage

Chemical class

Benzene carboxamides

Molecular weight

290.31 g/mol

Usage

Intermediate in the production of dyes, pigments, and optical brighteners

Application

Building block in the synthesis of various polymers and advanced materials

Potential applications

Pharmaceuticals and biomedicine

Toxicity

Low toxicity, not acutely harmful to human health or the environment

Upstream product

• 750-09-4 N,N'-Bis-(2-nitro-phenyl)-isophthalamide 
• 121-91-5 isophthalic acid 
• 95-54-5 1,2-diamino-benzene 
• 77929-24-9 [3-(2-Thioxo-thiazolidine-3-carbonyl)-phenyl]-(2-thioxo-thiazolidin-3-yl)-methanone 

Downstream Products

• 1217890-40-8 C₃₄H₂₆N₄O₄ 

Relevant academic research and scientific papers

Synthesis of novel acyclic and multiple phenyl iron tetraamino ligand catalysts and its catalytic activity for degradation of dye wastewater by H2O2

We need a practical, inexpensive, and green way to reduce the environmental pollutants, especially for dye wastewater. The discharge of industrial wastewater such as organic dyes will cause serious pollution to water bodies, thereby affecting people's liv

Photochromism of Schiff base compounds derived from N,N'-bis(2-aminophenyl) isophthalamide: Structure and photosensitivity

The photochromic behaviors of four Schiff bases derived from N,N'-bis(2-aminophenyl)isophthalamide were studied to reveal the substituent effect on the photosensitivity. On UV radiation, all of compounds 1-4 exhibit photochromic behavior in solution throu

Beneficial effect of Mukaiyama reagent on macrobislactamization reactions

An expeditious two-step procedure was developed to accede to new tetraamide macrocycles. The key step of this diversity-oriented procedure is a highly efficient Mukaiyama salt promoted macrobislactamization. Preliminary mechanistic investigations are also

Desymmetrization reactions: A convenient synthesis of aromatic diamide diamines

A two-step process for the synthesis of various diamide diamines derived from 1,n-diamino benzene compounds is described. The amidation reaction is simple, mild, involves readily available bis(N-acylthiazolidine-2-thione) derivatives as acylating agents and requires only stoichiometric equivalents of diamine and acylating agents.