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6-(hydroxymethyl)-9-methoxyphenazine-1-carboxylic acid is a complex organic compound with the molecular formula C14H13N2O4. It is characterized by a phenazine core, which is a tricyclic system with a central pyrazine ring and two benzene rings attached to it. The compound features a hydroxymethyl group (-CH2OH) at the 6th position and a methoxy group (-OCH3) at the 9th position, which are both substituents that can influence the compound's reactivity and properties. The carboxylic acid group (-COOH) at the 1st position provides the molecule with acidic properties, allowing it to participate in various chemical reactions, such as forming salts or esters. 6-(hydroxymethyl)-9-methoxyphenazine-1-carboxylic acid may have potential applications in pharmaceuticals, dyes, or other industrial processes, but its specific uses and properties would depend on further research and development.

489-76-9

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489-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 489-76-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 489-76:
(5*4)+(4*8)+(3*9)+(2*7)+(1*6)=99
99 % 10 = 9
So 489-76-9 is a valid CAS Registry Number.

489-76-9Upstream product

489-76-9Downstream Products

489-76-9Relevant academic research and scientific papers

New anticancer antibiotics pelagiomicins. Produced by a new marine bacterium Pelagiobacter variabilis

Imamura, Nobutaka,Nishijima, Miyuki,Takadera, Takahide,Adachi, Kyoko,Sakai, Miho,Sano, Hiroshi

, p. 8 - 12 (1997)

In the course of our screening for new anticancer compounds produced by marine bacteria, we found that a new genus marine bacterium Pelagiobacter variabilis produced new phenazine antibiotics, pelagiomicins A, B and C. Those compounds were labile in water and alcohols. The absolute structure of the main component, pelagiomicin A, and the structures of the minor ones were determined from the spectroscopic data and by synthesis. Pelagiomicin A exhibits activity against Gram-positive and-negative bacteria and antitumor activity in vitro and in vivo.

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