5520-63-8

Usage

Chemical structure

TATD is a positively charged polycyclic compound with a cyclic structure.

Application

It is used as a high-energy density material in the formulation of insensitive high explosives.

Potential replacement

TATD is considered to be a potential replacement for nitroaromatic explosives due to its lower sensitivity to impact and friction.

Nitrogen content

TATD has a high nitrogen content, which contributes to its explosive properties.

Thermal stability

TATD has been studied for its thermal stability.

Detonation performance

TATD has been studied for its detonation performance.

Potential applications

TATD has potential applications in military and civilian industries.

Cationic compound

As a cationic compound, TATD is also a potential candidate for pharmaceutical and medicinal applications.

Unique structure and properties

TATD has a unique structure and properties, which makes it a potential candidate for pharmaceutical and medicinal applications.

Upstream product

• 100-97-0 hexamethylenetetramine 
• 135-73-9 2-Bromo-4'-phenylacetophenone 

Downstream Products

• 71350-68-0 2-Amino-1-biphenyl-4-yl-ethanone; hydrochloride 
• 154532-13-5 4'-<(4-phenylbenzoylmethyl)aminocarbonyl>-4-(5-phenyl-1,3,4-oxadiazol-2-yl)biphenyl 

Relevant academic research and scientific papers

Investigations into the parallel synthesis of novel pyrrole-oxazole analogues of the insecticide pirate

Investigations into the parallel synthesis of selected analogues of a structurally unique pyrrole-oxazole analogue of the pyrrole insecticide pirate, are reported. Acylaminoketone salts were obtained from ketobromides in moderate to high yields and excell

SYNTHESIS OF LUMINOPHORIC DERIVATIVES OF PBD BASED ON 2,5-DIARYL SUBSTITUTED THIAZOLES AND OXAZOLES

The Friedel-Crafts acylation of 2-(biphenyl-4-yl)-5-phenyl-1,3,4-oxadiazole (PBD) with hippuryl chloride has been used to prepare the derivative V which on cyclization with POCl3 or P4S10 gives the respective oxazole (or thiazole) derivative of PBD, XIa or XIb.The reaction of carboxylic acid II with 4-(ω-aminoacetyl)biphenyl in the presence of CDI gives N-acyl-α-aminoketone VII; the analogous compound VI has been prepared by acylating ω-aminoacetophenone with acyl chloride III.The cyclization of these compounds gives bifluorophores Xa - Xd.

New biphenyl derivatives II: 1-(4-biphenylyl)-1-hydroxy-2-aminoethanes and 1-(4-biphenylyl)-1-chloro-2-aminoethanes as potential β-adrenoceptor blocking agents

Series of 1-(4-biphenylyl)-1-hydroxy-2-aminoethanes and 1-(4-biphenylyl)-1-chloro-2-aminoethanes were synthesized. Newly developed reaction conditions for aryl aminomethyl ketone reduction and reductive alkylation, using sodium borhydride, are described. The prepared compounds were examined for adrenergic blocking activity on an anesthetized dog blood pressure preparation and on isolated toad hearts. β-adrenergic blockade was investigated using isoproterenol as the agonist. The benzylamino and cyclohexylamino analogs exhibited marked β-adrenoceptor blocking activity, for which the latter derivatives were more potent.