39143-47-0

Upstream product

• 50626-23-8 5-(4-nitrophenyl)-2-phenyl-2H-tetrazole 
• 20147-55-1 p-nitrobenzaldehyde phenylhydrazonoyl chloride 
• 39718-99-5 N-anilino-4-nitrobenzamide 
• 20147-55-1 N-phenyl-p-nitrobenzhydrazonoyl chloride 

Downstream Products

• 85093-08-9 C₁₄H₉ClN₄O₅S 
• 130542-46-0 C₂₉H₂₁N₃O₃S 
• 104861-07-6 (3aS,4S,5R,9bS)-4-Isopropyl-5-methyl-1-(4-nitro-phenyl)-3-phenyl-3a,4,5,9b-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline 
• 130542-52-8 2-(4-Nitro-phenyl)-1,4-diphenyl-4H-10-thia-3,4-diaza-phenanthrene 
• 51128-78-0 C₂₆H₂₁N₄O₄P 
• 51128-69-9 6-(4-nitro-phenyl)-2,5,5-triphenyl-2H-5λ⁵-[1,2,4,5]triazaphosphinin-3-one 

Relevant academic research and scientific papers

Regioselective 1,3-dipolar cycloaddition of nitrilimines to 2-methyl-2-vinyl oxirane

1,3-Dipolar cycloaddition of in situ generated C,N-diaryl nitrilimines to 2-methyl-2-vinyl oxirane gives rise to the regioselective formation of novel 5-(2-methyloxiranyl)-4,5-dihydropyrazole derivatives in moderate to good yields. The structures and ster

Synthesis of 1,3,4-thiadiazolines from 1,2-dithiole-3-thiones

The thiocarbonyl group of 4,5-dichloro-1,2-dithiole-3-thione reacts as a 1,3-dipolarophile towards diaryl nitrile imines by 1,3-dipolar cycloaddition followed by opening of the dithiole ring with loss of sulfur to give 5-methylene-1,3,4-thiadiazolines; th

Ketoken gem-dithiols and trithiones: Synthesis and study of the behavior towards dipole reagents; Synthesis of some nitrogen heteroaromatics

The behavior of ketoken gem-dithiols towards active methylene and methyl groups resulted in the formation of thiopyrano-dihydrocaumarine derivatives IIIa,b via cyclocondensation reaction between substituted 4-dihydrocyclohexanone Ia.b. N-phenylpyrazoline

Photochemistry of Diarylsubstituted 2H-Tetrazoles, XI and Sydnones. V. Flashphotolytic Investigations with 2,5-Diaryl-2H-tetrazoles and 3,4-Diarylsydnones. Absolute Rate Constants of Cycloadditionreactions of Diarylnitrile Imines to Dipolarophils

The flash photolysis of 2,5-Diaryl-2H-tetrazoles 1 and 3,4-Diarylsydnones 2 was investigated.The nitrile imines were detected spectroscopically as short living intermediates.Rate constants of the cycloaddition reaction of nitrile imines and dipolarophiles

Photochemistry of Diarylsubstituted 2H-Tetrazoles. II. The Influence of the Substituents on the Absorption Properties of Diarylsubstituted Nitrilimines

Irradation of 2,5-diaryl-2H-tetrazoles in an EPA-glass (ether: i-pentan: ethanol = 5:5:2) or in an i-pentan glass at 77-80 K with UV-light of wavelength 290 nm yields diarylnitrilimines by the extrusion of nitrogen.The photoreactions investigated show spe