13158-31-1

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is the widely recognized name for the compound, which is derived from its structural features.

Explanation

It is used to harden or cure epoxy resins, which are essential in various industrial applications.

Explanation

It serves as a starting material or building block for the synthesis of other organic compounds.

Explanation

The compound's color and crystalline structure are important characteristics for its identification and handling.

Explanation

This property determines the compound's compatibility with different solvents, which is crucial for its application in various chemical processes.

Explanation

The compound's ability to withstand high temperatures without decomposing makes it suitable for use in high-temperature applications.

Explanation

Due to its properties, it is widely used in the manufacturing of various industrial products, including adhesives, coatings, and composite materials.

Explanation

It is essential to handle this chemical with care and follow safety guidelines to prevent potential health risks.

Use

Curing agent for epoxy resins

Use

Chemical intermediate in the production of organic compounds

Physical appearance

White to light yellow crystalline powder

Solubility

Insoluble in water, soluble in organic solvents

Thermal stability

High

Applications

Production of adhesives, coatings, and composite materials

Safety precautions

Harmful if ingested, inhaled, or in contact with the skin

Upstream product

• 124-40-3 dimethyl amine 
• 100-20-9 terephthaloyl chloride 
• 680-31-9 N,N,N,N,N,N-hexamethylphosphoric triamide 
• 100-21-0 terephthalic acid 
• 68-12-2 N,N-dimethyl-formamide 
• 127-19-5 N,N-dimethyl acetamide 
• 16766-91-9 1,4-bis(tribromomethyl)benzene 
• 120-61-6 1,4-benzenedicarboxylic acid dimethyl ester 

Downstream Products

• 66661-50-5 N,N,N',N'-Tetrakis-chloromethyl-terephthalamide 
• 121234-70-6 Terephthalsaeure-bis- 
• 66661-52-7 N,N,N',N'-Tetrakis-methoxymethyl-terephthalamide 
• 623-27-8 terephthalaldehyde, 

Relevant academic research and scientific papers

Metal-Free Amidation of Acids with Formamides and T3P

A new, simple and metal-free method for the direct formation of dialkylamides from carboxylic acids employing N,N-dialkylformamides as amine source is described. The one-pot reaction is promoted by propylphosphonic anhydride (T3P) in the presence of 0.5 equivalents of HCl.

A novel method for the conversion of carboxylic acids to N,N-dimethylamides using N,N-dimethylacetamide as a dimethylamine source

A simple, cost effective and environmentally benign method is reported for the preparation of N,N-dimethylamides from carboxylic acids. The versatility of the method is determined by synthesising a large number of N,N-dimethylamide derivatives. Carboxylic acids are heated at 160-165°C in N,N-dimethylacetamide solvent in the presence of1,1'-carbonyldiimidazole to afford the corresponding N,N-dimethylamides in good to excellent yields.

An effective synthesis of N,N-dimethylamides from carboxylic acids and a new route from N,N-dimethylamides to 1,2-diaryl-1,2-diketones

Carboxylic acids were heated at 150 °C in DMF in the presence of 1.25 equiv of thionyl chloride to give corresponding N,N-dimethylamides in good yields. Tandem chlorination and amidation reactions occurred in the one-pot procedure. Dicarboxylic acids needed prolonged reaction time to produce bisamides in good yields. Some benzamides were efficiently converted into corresponding 1,2-diaryl-1,2-diketones (benzils) under acyloin condensation conditions in the presence of 4,4′-di-tert-butylbiphenyl (DBB) in THF. Ultrasonic irradiation effectively accelerates the reaction, but it is not critical. However, the presence of DBB is fatal to the reaction. Although a few synthetic methods for benzils from benzoic acids have been reported so far, this method is one of the most convenient and highly reproducible procedures.

Method for the synthesis of amides and related products from esters or ester-like compounds

A versatile, eco-friendly, and efficient method for the convenient conversion of esters and ester-like compounds into amides, peptides, carbamates, ureas, oxamides, oxamates, hydrazides, oxazolidinones, pyrazolones, oxazolidinediones, barbituric acids, and other molecules containing one or more OCN moieties in the presence of a diol or polyol is disclosed.

Palladium(0) complex-catalyzed debrominative coupling of (tribromomethyl)- and (dibromomethyl)benzenes to diarylacetylenes and 1,2-diarylethenes

Palladium(0)-triphenylphosphine complex-catalyzed debrominative coupling reaction of (tribromomethyl)benzenes gave diarylacetylenes or a mixture of (E)- and (Z)-α,β-dibromostilbenes depending upon the substrate and the solvent being used. On the other hand, (dibromomethyl)benzenes afforded (E)-stilbenes selectively under the same reaction conditions.