710300-01-9

Upstream product

• 6628-86-0 5-chloro-2-nitrobenzaldehyde 
• 1445859-26-6 C₉H₈ClNO₃ 

Downstream Products

• 710300-10-0 ethyl 3-(5-chloro-2-nitrobenzoyl)-Δ²-pyrazoline-5-carboxylate 
• 873465-45-3 N-[3-(5-chloro-2-nitrophenyl)-3-oxopropyl]phthalimide 
• 873465-58-8 N-[3-(5-chloro-2-nitrophenyl)-3-oxopropyl]cyclopropanecarboxamide 
• 873465-59-9 N-[3-(5-chloro-2-nitrophenyl)-3-oxopropyl]benzamide 
• 873465-47-5 N-[3,3-ethylenedioxy-3-(5-chloro-2-nitrophenyl)propyl]phthalimide 
• 710300-48-4 ethyl 1-acetyl-3-(5-chloro-2-nitrobenzoyl)-Δ²-pyrazoline-5-carboxylate 
• 710300-51-9 ethyl 3-(5-chloro-2-nitrobenzoyl)-1-propionyl-Δ²-pyrazoline-5-carboxylate 
• 710300-54-2 ethyl 1-butyryl-3-(5-chloro-2-nitrobenzoyl)-Δ²-pyrazoline-5-carboxylate 
• 710300-56-4 ethyl 3-(5-chloro-2-nitrobenzoyl)-1-pentanoyl-Δ²-pyrazoline-5-carboxylate 
• 710300-71-3 ethyl 1-benzoyl-3-(5-chloro-2-nitrobenzoyl)-Δ²-pyrazoline-5-carboxylate 
• 710300-62-2 ethyl 3-(5-chloro-2-nitrobenzoyl)-1-cyclobutanecarbonyl-Δ²-pyrazoline-5-carboxylate 
• 710300-65-5 ethyl 3-(5-chloro-2-nitrobenzoyl)-1-cyclopentanecarbonyl-Δ²-pyrazoline-5-carboxylate 
• 710300-68-8 ethyl 3-(5-chloro-2-nitrobenzoyl)-1-cyclohexanecarbonyl-Δ²-pyrazoline-5-carboxylate 

Relevant academic research and scientific papers

Thiadiazoline- And pyrazoline-based carboxamides and carbothioamides: Synthesis and inhibition against nitric oxide synthase

Two new families of pyrazoline and thiadiazoline heterocycles have been developed. Their inhibitory activities against two different isoforms of nitric oxide synthase (inducible and neuronal NOS) are reported. The novel derivatives were synthesized combining the arylthiadiazoline or arylpyrazoline skeleton and a carboxamide or carbothioamide moiety, used as starting material ethyl 2-nitrobenzoates or substituted nitrobenzaldehydes, respectively. The structure-activity relationships of final molecules are discussed in terms of the R1 radical effects in the aromatic ring, the Y atom in the heterocyclic system, the X heteroatom in the main chain, and the R2 substituent in the carboxamide or carbothioamide rest. In general, thiadiazolines (5a-e) inhibit preferentially the neuronal isoform; among them, 5a is the best nNOS inhibitor (74.11% at 1 mM, IC50 = 420 M). In contrast, pyrazolines (6a-r) behave better as iNOS than nNOS inhibitors, 6m being the best molecule of this series (76.86% at 1 mM of iNOS inhibition, IC50 = 130 M) and the most potent of all tested compounds.

Synthesis and biological evaluation of 4,5-dihydro-1H-pyrazole derivatives as potential nNOS/iNOS selective inhibitors. Part 2: Influence of diverse substituents in both the phenyl moiety and the acyl group

In a preliminary article, we reported a series of 4,5-dihydro-1H-pyrazole derivatives as neuronal nitric oxide synthase (nNOS) inhibitors. Here we present the data about the inhibition of inducible nitric oxide synthase (iNOS) of these compounds. In gener

N-PHENYL-1,1,1-TRIFLUOROMETHANESULFONAMIDE HYDRAZONE DERIVATIVE COMPOUNDS AND THEIR USAGE IN CONTROLLING PARASITES

Novel N-phenyl-1,1,1-trifluoromethanesulfonamide compounds useful for controlling endo and/or ectoparasites in the environment are provided, together with methods of making the same, and methods of using the inventive compounds to treat parasite infestations in vivo and ex vivo.