ChemInform Abstract: Synthesis of Azo Compounds Containing Thymol Moiety.

Koshti, S. M.; Sonar, J. P.; Sonawane, A. E.; Pawar, Y. A.; Nagle, P. S.; Mahulikar, Pramod P.; More, Dhananjay H.

doi:10.1002/chin.200823176

Cited by 4 publications

(3 citation statements)

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“…The role that thymol plays in medicinal chemistry has inspired numerous researchers to explore its wide range of biological activities. Numerous thymol derivatives have been developed and evaluated for their biological characteristics; we can specifically mention glucosides [ 93 ], Mannich bases [ 94 ], ethers [ 95 ], aldehydes [ 96 ], esters [ 97 ], azo dyes [ 98 ], and formylation products [ 99 ]. According to Desai et al, thymol moiety linked to pyrazole, isoxazole, and pyridine motifs produced compounds with promising antimicrobial activities [ 100 ].…”

Section: Natural Productsmentioning

confidence: 99%

Antifungal Activities of Natural Products and Their Hybrid Molecules

Khwaza,

Aderibigbe

2023

Pharmaceutics

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The increasing cases of drug resistance and high toxicity associated with the currently used antifungal agents are a worldwide public health concern. There is an urgent need to develop new antifungal drugs with unique target mechanisms. Plant-based compounds, such as carvacrol, eugenol, coumarin, cinnamaldehyde, curcumin, thymol, etc., have been explored for the development of promising antifungal agents due to their diverse biological activities, lack of toxicity, and availability. However, researchers around the world are unable to fully utilize the potential of natural products due to limitations, such as their poor bioavailability and aqueous solubility. The development of hybrid molecules containing natural products is a promising synthetic approach to overcome these limitations and control microbes’ capability to develop resistance. Based on the potential advantages of hybrid compounds containing natural products to improve antifungal activity, there have been different reported synthesized hybrid compounds. This paper reviews different literature to report the potential antifungal activities of hybrid compounds containing natural products.

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Section: Natural Productsmentioning

confidence: 99%

Antifungal Activities of Natural Products and Their Hybrid Molecules

Khwaza,

Aderibigbe

2023

Pharmaceutics

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“…3 Azo dyes, shows wide application in many fields like dyeing textile fibres, biomedical studies, advanced applications in organic synthesis & high technology areas like lasers, liquid crystalline displays, electro-optical devices & ink-jet printers. [4][5] Some azo dye possess medicinal properties like antiseptic, antiprotzoal, antifungal, antibacterial and dyes antipyretic properties. [6][7][8][9] Azo dyes are the largest & most important class of organic dyestuffs.…”

Section: Introductionmentioning

confidence: 99%

Synthesis & Characterization Of Azo Compounds Containing Disubstituted Phenolic Moities

Lokhande¹,

Thakare²

2019

International Journal of Advanced Scientific Research and Management

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Dyes are organic compounds which gives colour to a substrate. Azo dyes are the largest group of colorants used in industry. Due to their ability to absorb visible light & ease of synthesis dyes have wider industrial application and use such as textiles, fiber, leather, print and painting, also in agriculture, cosmetics & in laboratories. In this research eight azo compounds are prepared by diazo coupling. The diazotizonium salt is formed when NaNO 2 & concentrated HCl is treated with substituted aromatic amines viz. Aniline, Anthranilic acid, α-Naphathalamine, Benzidene, o-Nitroaniline, p-nitroaniline, sulphanilic acid and ptoulidine. The formation of novel dye took place with a sufficient yield with subsequent coupling of 2,4-dimethylphenol. The structures of prepared dyes are confirmed by Fourier transform Infrared & proton nuclear magnetic resonance spectroscopy. Perkin Elmer spectrum used for IR spectra & Bruker Avance 400MHz NMR spectrometer for NMR spectra. The IR spectra showed 3000-3500cm-1 streching for hydroxyl group & 1405-1550cm-1 streching for-N=Nbond and mass of azo compound found to be m/z 304(M+).

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“…For improving the survival ability and penetration ability of weapon equipment, the simple and effective method is coating the infrared stealth materials on the surface of the weapons [1] .Phase change materials is a kind of material which can store and release energy in the form the latent heat without any temperature change of its own [2] . By using of microcapsule technical to encapsulate the phase change material and then covering with coatings on target, we can proceed with the simulation of background infrared characteristics and get the best infrared stealth effect by controlling the target surface thermal inertia and surface temperature, eliminating or reducing the target and background of infrared radiation difference [3][4][5] .…”

Section: Introductionmentioning

confidence: 99%

Preparation of Infrared Stealthy Coatings

Cui

Yang

et al. 2013

AMM

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Two kinds of microcapsules were synthesized with paraffin and the mixture of n-butyl stearate and n-tetradecyl alcohol as the core material, and the melamine-formaldehyde (MF) resin as shell material, respectively. In this way, the infrared stealthy coatings were prepared by using the as-synthesized microcapsules, the hollow glass microspheres and other auxiliaries. The surface morphology of the microcapsules were investigated by using scanning electron microscopy (SEM). By using the contactless infrared thermometer measurement and radiation rate test device, the radiation exitances of coatings were determined. The radiation exitance of infrared stealthy coatings is lower than the common coatings, which improved the performance of infrared stealthy of destination.

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ChemInform Abstract: Synthesis of Azo Compounds Containing Thymol Moiety.

Cited by 4 publications

References 0 publications

Antifungal Activities of Natural Products and Their Hybrid Molecules

Antifungal Activities of Natural Products and Their Hybrid Molecules

Synthesis & Characterization Of Azo Compounds Containing Disubstituted Phenolic Moities

Preparation of Infrared Stealthy Coatings

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