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2',5'-dihydroxyacetophenone isonicotinoyl hydrazone is a complex organic compound with the molecular formula C15H14N2O3. It is a derivative of acetophenone, featuring two hydroxyl groups at the 2' and 5' positions, and an isonicotinoyl hydrazone moiety. 2',5'-dihydroxyacetophenone isonicotinoyl hydrazone is known for its potential applications in the field of chemistry, particularly as a synthetic intermediate or a building block for more complex molecules. Its structure and properties make it a subject of interest for researchers exploring the synthesis and reactivity of organic compounds. The compound's name reflects its chemical structure, indicating the presence of a hydrazone group derived from isonicotinic acid (isonicotinoyl) bonded to a modified acetophenone molecule with hydroxyl substitutions.

895-06-7

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895-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 895-06-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 895-06:
(5*8)+(4*9)+(3*5)+(2*0)+(1*6)=97
97 % 10 = 7
So 895-06-7 is a valid CAS Registry Number.

895-06-7Downstream Products

895-06-7Relevant academic research and scientific papers

Synthesis of metal-based analogues of isonicotinoyl and benzoyl hydrazones and their antioxidant and cytotoxic activities

Shafiq, Zahid,Hussain, Mazhar,Yaqub, Muhammad,Shafiq, Kiran,Ashraf, Mohammad,Ahmad, Hafiz Badaruddin

experimental part, p. 4623 - 4628 (2012/08/28)

A series of 20 metal based [Cu(II), Co(II), Ni(II), Mn(II) and Zn(II)] compounds have been synthesized with novel 2,5-dihydroxyacetophenone isonicotinoyl hydrazone (L1) and 2,5-dihydroxyacetophenone benzoyl hydrazone (L2) Schiff bases and were screened for antioxidant and cytotoxic activities. All these complexes exhibited strong antioxidant activity against DPPH radical but no nitric oxide radical scavenging activity. Cytotoxicity assay showed toxicity at varied levels, that is, 1, 3, 7, 11, 15 showed maximum toxicity and 4, 9, 10, 12, 13, 16, 19, 20 showed minimal cytotoxicity against brine shrimp larvae. Antibacterial activity assay exhibited MIC50 values of 2, 4, 6, 8, 10, 12, 14, 16, 18, 20 comparable to standard drugs for both gram-positive and gram-negative bacteria whilst other compounds showed minimal activity against these bacteria. Structure activity relationship shows the role of metal and the kind of complex associated with the said biological activities.

Synthesis of hydrazones schiff bases and microbiological evaluation of lsonicotinoyl hydrazide with different acetophenone

Kelode,Mandlik,Aswar

scheme or table, p. 1053 - 1062 (2012/04/04)

A series of hydrazones Schiff bases compounds have been synthesized by reacting isonicotinoyl hydrazide with 2-hydroxy-5-chloro acetophenone, 2-hydroxy-5-methyl acetophenone, 2-hydroxy-5-carboxy acetophenone, 2,5-dihydroxy acetophenone, 2-hydroxy-5-chloro-4-methyl acetophenone, 2-hydroxy-5-chloro-3- nitro acetophenone, 2-hydroxy-5-methyl-3-nitro acetophenone and 2-hydroxy-5-bromo acetophenone. The Schiff bases have been evaluated for the antifungal and antibacterial activities.

Schiff base metal complexes of chromium(III), manganese(III), iron(III), oxovanadium(IV), zirconium(IV) and dioxouranium(VI)

Mandlik,Aswar

, p. 129 - 135 (2007/10/03)

The Schiff base 2,5-dihydroxyacetophenone isonicotinoyl hydrazone (H2L) has been synthesized by condensation of 2,5-dihydroxyacetophenone with isonicotinoyl hydrazide in ethanol. Metal complexes of the Schiff base were prepared from salts of Cr

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