62812-80-0

Upstream product

• 1779-81-3 4,5-Dihydro-thiazol-2-ylamin 
• 122-04-3 4-nitro-benzoyl chloride 
• 151-56-4 ethyleneimine 
• 90964-35-5 (4-nitro-benzoyl)-dithiocarbamic acid methyl ester 
• 156-57-0 2-mercaptoethylamine hydrochloride 
• 74074-24-1 N-(Bis-methylsulfanyl-methylene)-4-nitro-benzamide 
• 76098-31-2 N-(4-Nitrobenzoyl)-1-pyrrolidinecarbimidoyl Chloride 
• 60-23-1 Cysteamine 
• 28115-92-6 4-nitrobenzoyl isothiocyanate 

Relevant academic research and scientific papers

Ring-opened analogs of indomethacin affecting human neutrophil functions

A series of ring-opened analogs of indomethacin was synthesized and tested in vitro (at concentrations ranging from 10-9 to 10-5 mol/1) on human neutrophil functions. Two compounds lacking the carboxylic group were subjected to the s

Synthesis of 6,7-dihydrothiazolo[3,2-a]-1,3,5-triazine-4-aryl-2-thiones

Reaction of 2-aminothiazoline with aroylisothiocyanate gave 6,7-dihydrothiazolo[3,2-a]-1,3,5-triazine-4-aryl-2-thiones (5) in one step.

Tautomerie von Heterocyclen, VIII. N-Acylsubstituierte Chlorformamidine als Heterocyclen- Bausteine

N-(4-Nitrobenzoyl)-1-pyrrolidinecarbimidoyl chloride (1) reacts with bisnucleophilic reagents according to two possible pathways to differently structured heterocyclic compounds.In path A following the substitution of the chlorine atom ring closure from t

2-Aminothiazoline derivatives. Relationships between structure and antiinflammatory activity

Pharmacological studies of 2-aminothiazoline amide and amine derivatives show these compounds to be actively anti-inflammatory. The structure determination by spectroscopic methods and X-ray diffraction indicates a relation between the structure and the activity of these compounds.