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3-Hydroxy-N-(p-methoxybenzyl)-picolinamid is a chemical compound with the molecular formula C15H16N2O3. It is a derivative of picolinic acid, featuring a hydroxyl group at the 3-position and a p-methoxybenzyl group attached to the nitrogen atom. 3-Hydroxy-N-(p-methoxybenzyl)-picolinamid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and drugs. Its structure provides a unique combination of functional groups that can be further modified or reacted to yield a range of products with different properties and uses.

1089-26-5

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1089-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1089-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1089-26:
(6*1)+(5*0)+(4*8)+(3*9)+(2*2)+(1*6)=75
75 % 10 = 5
So 1089-26-5 is a valid CAS Registry Number.

1089-26-5Downstream Products

1089-26-5Relevant academic research and scientific papers

Antimycobacterial and antifungal isosters of salicylamides

Waisser, Karel,Pe?ina, Milan,Holy, Pavel,Pour, Milan,Bure?, Otakar,Kune?, Ji?í,Klime?ová, V?ra,Buchta, Vladimír,Kubanová, Petra,Kaustová, Jarmila

, p. 322 - 335 (2007/10/03)

A set of 40 derivatives of 3-hydroxypicolinic acid and 2-sulfanylbenzoic acid, isosteric to salicylanilides was synthesized. The compounds were evaluated for in vitro activity against Mycobacterium tuberculosis, Mycobacterium kansasii and Mycobacterium avium, Candida albicans, Candida tropicalis, Candida krusei, Candida glabrata, Trichosporon beigelii, Aspergillus fumigatus, Absidia corymbifera, Trichophyton mentagrophytes and Microsporum gypseum. Structure-activity relationships of antimycobacterial activity and antifungal activity against T. mentagrophytes and M. gypseum were analyzed by the Free-Wilson method. An increase in antimycobacterial activity was observed only for the sulfanylbenzoic acid derivatives, especially those with the benzyl moiety. The antifungal activity was not significant.

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