19368-13-9

Upstream product

• 85-44-9 phthalic anhydride 
• 99-92-3 p-aminobenzophenone 
• 14235-81-5 4-Ethynylaniline 

Downstream Products

• 40101-59-5 2-(4-acetylphenyl)-1H-isoindole-1,3(2H)-dione 
• 1416218-06-8 C₂₇H₂₀N₄O₄ 
• 1416218-07-9 C₂₃H₁₉N₃O₃ 
• 1416218-08-0 C₂₃H₁₈ClN₃O₃ 
• 1416218-09-1 C₂₄H₂₁N₃O₄ 
• 1416218-10-4 C₂₉H₂₃N₃O₃ 
• 1416218-11-5 C₂₉H₂₂ClN₃O₃ 
• 1416217-95-2 2-((4-(1-(2-phenylhydrazono)ethyl)phenyl)carbamoyl)benzoic acid 
• 1416217-96-3 2-((4-(1-(2-carbamoylhydrazono)ethyl)phenyl)carbamoyl)benzoic acid 
• 1429492-72-7 2-((4-(1-(2-benzoylhydrazono)ethyl)phenyl)carbamoyl)benzoic acid 
• 1416217-98-5 2-(4-cinnamoylphenylcarbamoyl)benzoic acid 
• 1416218-01-3 C₂₆H₁₇N₃O₄ 
• 1416218-04-6 C₂₆H₁₈N₄O₃ 
• 1416217-99-6 2-(4-(3-(4-chlorophenyl)acryloyl)phenylcarbamoyl)benzoic acid 

Relevant academic research and scientific papers

Compounds and methods for inducing chondrogenesis

The present invention provides compounds and compositions for the amelioration of arthritis and joint injuries by inducing mesenchymal stem cells into chondrocytes.

Computational modeling, synthesis, and antioxidant potential of novel phenylcarbamoylbenzoic acid analogs in combating oxidative stress

A new series of phenylcarbamoylbenzoic acid analogs were designed, synthesized, and evaluated for their in vitro antioxidant activity, aiming to find a lead for the treatment of oxidative stress. The target compounds were prepared by substituting the core

Thermal Reaction of Ethynylphthalimides and Hydration of N-(4-Ethynylphenyl)phthalimide

Three ethynyl substituted phenylphthalimides were prepared and characterized by high pressure liquid chromatography, differential scanning calorimetry, and mass spectroscopy.When the preparation of N-(4-ethynylphenyl)phthalimide was attempted by the thermal cyclodehydration of N-(4-ethynylphenyl)-2-carboxybenzamide, N-(4-acetylphenyl)phthalimide was obtained as the major component.This unusual hydration of an ethynyl group was investigated and a mechanism was proposed to explain it.