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3-Hydroxy-4-methoxy-benzaldehyde-(2,4-dinitro-phenylhydrazone) is a complex organic compound with the molecular formula C15H14N4O6. It is derived from 3-hydroxy-4-methoxy-benzaldehyde, a naturally occurring aromatic aldehyde, by forming a hydrazone with 2,4-dinitrophenylhydrazine. 3-hydroxy-4-methoxy-benzaldehyde-(2,4-dinitro-phenylhydrazone) is characterized by its yellow crystalline appearance and is soluble in common organic solvents. It is often used in chemical research and analysis, particularly in the identification and characterization of aldehydes and ketones due to the formation of colored hydrazones. The 2,4-dinitrophenylhydrazone derivative provides a convenient way to study the parent aldehyde, as the resulting compound is more stable and easier to handle than the aldehyde itself.

1166-14-9

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1166-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1166-14-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1166-14:
(6*1)+(5*1)+(4*6)+(3*6)+(2*1)+(1*4)=59
59 % 10 = 9
So 1166-14-9 is a valid CAS Registry Number.

1166-14-9Downstream Products

1166-14-9Relevant academic research and scientific papers

In vitro and in vivo anti-inflammatory properties of imine resveratrol analogues

Zimmermann-Franco, Danielle Cristina,Esteves, Bruna,Lacerda, Leticia Moroni,Souza, Isabela de Oliveira,Santos, Juliana Alves dos,Pinto, Nícolas de Castro Campos,Scio, Elita,da Silva, Adilson David,Macedo, Gilson Costa

, p. 4898 - 4906 (2018)

Resveratrol is a natural polyphenol found mainly on red grapes and in red wine, pointed as an important anti-inflammatory/immunomodulatory molecule. However, its bioavailability problems have limited its use encouraging the search for new alternatives agents. Thus, in this study, we synthetize 12 resveratrol analogues (6 imines, 1 thioimine and 5 hydrazones) and investigated its cytotoxicity, antioxidant activity and in vitro anti-inflammatory/immunomodulatory properties. The most promising compounds were also evaluated in vivo. The results showed that imines presented less cytotoxicity, were more effective than resveratrol on DPPH scavenger and exhibited an anti-inflammatory profile. Among them, the imines with a radical in the para position, on the ring B, not engaged in an intramolecular hydrogen-interaction, showed more prominent anti-inflammatory activity modulating, in vivo, the edema formation, the inflammatory infiltration and cytokine levels. An immunomodulatory activity also was observed in these molecules. Thus, our results suggest that imines with these characteristics presents potential to control inflammatory disorders.

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