41095-26-5

Basic information

• Product Name: Benzoic acid, 4-[(1-acetyl-2-oxopropylidene)hydrazino]-, ethyl ester
• CAS NO: 41095-26-5
• Molecular Formula: C14H16N2O4
• Molecular Weight: 276.292
• Mol File: 41095-26-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-[(1-acetyl-2-oxopropylidene)hydrazino]-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-[(1-acetyl-2-oxopropylidene)hydrazino]-, ethyl ester(41095-26-5)
• EPA Substance Registry System: Benzoic acid, 4-[(1-acetyl-2-oxopropylidene)hydrazino]-, ethyl ester(41095-26-5)

Safety Data

• Hazardous Substances Data: 41095-26-5(Hazardous Substances Data)

Upstream product

• 94-09-7 p-aminoethylbenzoate 
• 123-54-6 acetylacetone 
• 2028-79-7 4-(ethoxycarbonyl)benzenediazonium chloride 

Relevant articles and documents

Photoresponsive Zn2+-specific metallohydrogels coassembled from imidazole containing phenylalanine and arylazopyrazole derivatives

Stimuli-responsive supramolecular gels and metallogels have been widely explored in the past decade, but the fabrication of metallogels with reversible photoresponsive properties remains largely unexplored. In this study, we report the construction of pho

Synthesis and biological evaluation of new N-substituted-N′-(3,5-di/ 1,3,5-trimethylpyrazole-4-yl)thiourea/urea derivatives

Several thiourea and urea derivatives were prepared by the reaction of 4-aminopyrazoles with substituted isothiocyanates or isocyanates. The novel compounds were tested anticonvulsant activity using by pentylenetetrazole- induced seizure (PTZ) and maximal electroshock seizure (MES) tests. Among the tested compounds, thiourea derivatives of 4b were afforded 90 and 100% protection in PTZ and MES tests at 50 mg/kg, respectively. Urea derivatives of 5a and 5b were afforded 82 and 100% protection both at 25 and 50 mg/kg. Also synthesized compounds were screened for antituberculosis activity against Mycobacterium tuberculosis H37Rv at 6.25 μg/mL concentration but they were not found active at these concentration. In addition, some selected compounds were evaluated for in vitro anti-HIV activity and they were all negative.