4,4''-Dinitro-p-terphenyl, with the CAS number 3282-11-9, is an organic compound characterized by its structure, which consists of three phenyl rings connected by a central para-substituted phenyl group. This compound features two nitro groups (-NO2) positioned at the 4,4''-positions of the central phenyl ring, contributing to its chemical reactivity and properties. It is typically a yellow crystalline solid, exhibiting high thermal stability and relatively low solubility in water, but it can dissolve in organic solvents such as acetone and chloroform. 4,4''-Dinitro-p-terphenyl is known for its applications in the field of materials science, particularly as a high-energy material and in the development of explosives due to its energetic nitro groups. Additionally, it has been studied for its potential use in photonic applications and as a dye. Safety precautions are essential when handling this compound, as it may pose health risks and environmental hazards.

4,4''-Dinitro-p-terphenyl

3282-11-9: p-Terphenyl, 4,4''-dinitro-, 4,4''-Dinitro-1,1':4',1''-Terphenyl

4,4''-Dinitro-p-terphenyl is a pyridazine derivative that has been used in the synthesis of other organic compounds. It can be prepared by nitrating pyridine with 4,4''-dinitrobenzenesulfonyl chloride to give 4,4''-dinitropyridine, which is then treated with potassium hydroxide to produce 4,4''-dinitro-p-terphenyl. This molecule has solvents and temperatures that are suitable for use in various chemical reactions and can be used as an anion transfer reagent. The molecule has a cyclic structure and is susceptible to strain from electron delocalization or from the nitro groups on the ring.

4,4-DINITRO-P-TERPHENYL

4,4ÕÕ-Dinitro-1,1Õ:4Õ,1ÕÕ-Terphenyl

CAS 3282-11-9: 4,4''-Dinitro-p-terphenyl

4,4''-Dinitro-p-terphenyl

Ref: 3B-D3394

4,4''-Dinitro-p-terphenyl

Ref: 3D-FD62328

4,4-DINITRO-P-TERPHENYL

Ref: IN-DA003KGA

4,4ÕÕ-Dinitro-1,1Õ:4Õ,1ÕÕ-Terphenyl

Ref: 54-OR1029249