2372-71-6

Usage

Chemical compound

Yes

Usage

Crosslinking agent in polymer and resin manufacturing

Physical appearance

White to off-white powder

Molecular weight

378.35 g/mol

Primary uses

Curing agent, flame retardant, and crosslinking agent in polymer production

Polymer types

Polyurethanes, epoxy resins, and polyimides

Other applications

Adhesives, coatings, and sealants production

Potential uses

Corrosion inhibitor and additive in lubricants

Chemical structure

Consists of a 1,4-benzenedicarboxylic acid core with two 2-benzoylhydrazide groups attached.

Upstream product

• 613-94-5 benzoic acid hydrazide 
• 100-20-9 terephthaloyl chloride 
• 3477-75-6 1,3-bis(5-phenyl-1,3,4-oxadiazol-2-yl)benzene 
• 98-88-4 benzoyl chloride 
• 136-64-1 terephthalohydrazide 

Downstream Products

• 1266552-49-1 C₅₀H₅₆N₆ 
• 5888-97-1 5,5'-diphenyl-1,4-phenylenebis-1,3,4-oxadiazole 
• 17464-22-1 1,4-Bis-<5-phenyl-1,3,4-thiadiazolyl-(2)>-benzen 

Relevant academic research and scientific papers

Synthesis and nucleating effect of N, N'-Bis(Benzoyl) terephthalic acid dihydrazide

N, N'-Bis(benzoyl) terephthalic acid dihydrazide(NA) was synthesized from benzoyl hydrazine and terephthaloyl chloride which was deprived from terephthalic acid via acylation, and the structures of the synthesized compound had been characterized by Fourie

An Improved Synthesis of 1,3- and 1,4-Bisbenzenes via Oxidation of Bis-aroylhydrazones of Iso- and Terephthalaldehyde with Lead(IV) Acetate

The oxidation of bis-aroylhydrazones of iso- and terephthalaldehyde with lead(IV) acetate leading to 1,3- and 1,4-bisbenzenes is described.

Liquid Crystalline 1,3,4-Thiadiazoles. 1. Biphenyl- and Terphenyl Analogous 1,3,4-Thiadiazoles

The synthesis of disubstituted 1,3,4- and 1,2,4-thiadiazoles and 1,3,4-oxadiazoles is described and their melting and clearing points are investigated.The influence of the heterocyclic ring system on the formation of crystalline liquid phases is discussed