792-38-1

Basic information

• Product Name: N'-[1-(2,4-Dihydroxyphenyl)ethylidene]-4-pyridinecarbohydrazide
• Synonyms: N'-(2,4-Dihydroxy-α-methylbenzylidene)-4-pyridinecarbohydrazide;N'-(2,4-Dihydroxy-α-methylbenzylidene)isonicotinic hydrazide;N'-[1-(2,4-Dihydroxyphenyl)ethylidene]-4-pyridinecarbohydrazide;N'-[1-(2,4-Dihydroxyphenyl)ethylidene]isonicotinic hydrazide;Resacetophenone isoniazid hydrazone
• CAS NO: 792-38-1
• Molecular Formula: C₁₄H₁₃N₃O₃
• Molecular Weight: 0
• Mol File: 792-38-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N'-[1-(2,4-Dihydroxyphenyl)ethylidene]-4-pyridinecarbohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N'-[1-(2,4-Dihydroxyphenyl)ethylidene]-4-pyridinecarbohydrazide(792-38-1)
• EPA Substance Registry System: N'-[1-(2,4-Dihydroxyphenyl)ethylidene]-4-pyridinecarbohydrazide(792-38-1)

Safety Data

• Hazardous Substances Data: 792-38-1(Hazardous Substances Data)

Upstream product

• 54-85-3 isoniazid 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 1570-45-2 isonicotinic acid ethylester 
• 55-22-1 pyridine-4-carboxylic acid 

Downstream Products

• 89-84-9 2',4'-dihydroxy-4-acetophenone 

Relevant articles and documents

Complexation of N′-[1-(2,4-dihydroxyphenyl)ethylidene] isonicotinohydrazide with lanthanide ions

The complexation of N′-[1-(2,4-dihydroxyphenyl)ethylidene] isonicotinohydrazide (DEH) with trivalent Pr, Nd, Gd, Tb, and Ho ions were studied employing potentiometric and spectroscopic techniques. The potentiometric studies carried out at different temper

Synthesis, antimycobacterial, antiviral, antimicrobial activities, and QSAR studies of isonicotinic acid-1-(substituted phenyl)-ethylidene/cycloheptylidene hydrazides

A series of isonicotinic acid-1-(substituted phenyl)-ethylidene/ cycloheptylidene hydrazide derivatives (1-12) was tested for their, in vitro antimycobacterial activity against Mycobacterium tuberculosis, and compound 2 was found to be more active than isoniazid. The antiviral screening results indicated that none of the tested compounds was active against a broad variety of DNA and RNA viruses at subtoxic concentrations, except compounds 8 and 10 that proved to be active against DNA viruses at concentrations close to their cytostatic potential. The synthesized compounds were also screened for their antimicrobial potential against S. aureus, B. subtilis, E. coli, C. albicans and A. niger, and the results indicated that compounds having Br, OCH3 and Cl groups were highly active. The multi-target QSAR models indicated the importance of lipophilic (log P) and topological parameters (3vv) in describing the antimicrobial activity.

Synthesis, spectral, thermal, biological and 3D molecular modeling studies of oxidomolybdenum(V) and dioxidomolybdenum(VI) complexes derived from 2,4-dihydroxyacetophenone isonicotinoylhydrazone

Synthesis of some novel oxidomolybdenum(V) and dioxidomolybdenum(VI) complexes with a Schiff base, (2,4-dihydroxy acetophenoneisonicotinoylhydrazone) (DAIH), derived from 2,4-dihydroxy acetophenone and isonicotinoylhydrazide are reported. The complexes ha