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4-Pyridinecarboxylic acid, 2-[(2,4-dihydroxyphenyl)methylene]hydrazide, also known as isonicotinic acid 2-[(2,4-dihydroxyphenyl)methylene]hydrazide, is a chemical compound with the molecular formula C12H10N2O4. It is a derivative of pyridine, a heterocyclic aromatic compound, and features a hydrazide group attached to the pyridine ring. 4-Pyridinecarboxylicacid, 2-[(2,4-dihydroxyphenyl)methylene]hydrazide is characterized by the presence of two hydroxyl groups on the phenyl ring, which contributes to its chemical properties. It is an organic compound that can be used in the synthesis of various pharmaceuticals and has potential applications in the development of drugs targeting specific biological pathways. The compound's structure and properties make it a subject of interest in medicinal chemistry and drug design.

3477-69-8

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3477-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3477-69-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,7 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3477-69:
(6*3)+(5*4)+(4*7)+(3*7)+(2*6)+(1*9)=108
108 % 10 = 8
So 3477-69-8 is a valid CAS Registry Number.

3477-69-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[(E)-(2-hydroxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]pyridine-4-carbohydrazide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:3477-69-8 SDS

3477-69-8Downstream Products

3477-69-8Relevant academic research and scientific papers

Effective methods for the synthesis of hydrazones, quinazolines, and Schiff bases: Reaction monitoring using a chemometric approach

?ilovi?, Ivica,Cvijanovi?, Danijela,Hrenar, Tomica,Pavlovi?, Gordana,Pisk, Jana,Vrdoljak, Vi?nja

, p. 38566 - 38577 (2020/11/05)

Synthesis of hydrazones (1a-4a and 1b-4b), quinazolines (3c·MeOH and 3d·MeOH), and hydrazone-Schiff bases (4c and 4d) is achieved by combining suitable aldehydes (2,3- or 2,4-dihydroxybenzaldehyde) with four hydrazides (isonicotinic, nicotinic, and 2- or

Xanthine oxidase inhibitory activity of nicotino/isonicotinohydrazides: A systematic approach from in vitro, in silico to in vivo studies

Zafar, Humaira,Hayat, Muhammad,Saied, Sumayya,Khan, Momin,Salar, Uzma,Malik, Rizwana,Choudhary, M. Iqbal,Khan, Khalid Mohammed

, p. 2351 - 2371 (2017/04/03)

Change in life style and eating habits has led to an increased prevalence of hyperuricemia worldwide. The role of hyperuricemia is no more restricted to gout, but it has a central role in progression of CVD, hypertension, metabolic syndrome, and arthritis

Design, synthesis and in vitro antimalarial activity of an acylhydrazone library

Melnyk, Patricia,Leroux, Virginie,Sergheraert, Christian,Grellier, Philippe

, p. 31 - 35 (2007/10/03)

A library of acylhydrazone iron chelators was synthesized and tested for its ability to inhibit the growth of a chloroquine-resistant strain of Plasmodium falciparum. Some of these new compounds are significantly more active than desferrioxamine DFO, the

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