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8H-Pyrano[2,3-e]benzoxazol-8-one, 6-methyl-2-phenyl- is a complex organic compound with the molecular formula C16H11NO3. It is a derivative of the benzoxazole class of heterocyclic compounds, characterized by the presence of a benzene ring fused to an oxazole ring. The compound features a methyl group at the 6th position and a phenyl group at the 2nd position, which are both attached to the pyrano ring. This specific arrangement of functional groups gives the molecule unique chemical and physical properties, making it potentially useful in various applications, such as pharmaceuticals or materials science. The compound's structure and properties can be further explored through its chemical synthesis, spectroscopic analysis, and potential reactivity with other molecules.

3573-75-9

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3573-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3573-75-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3573-75:
(6*3)+(5*5)+(4*7)+(3*3)+(2*7)+(1*5)=99
99 % 10 = 9
So 3573-75-9 is a valid CAS Registry Number.

3573-75-9Downstream Products

3573-75-9Relevant academic research and scientific papers

New angular oxazole-fused coumarin derivatives: synthesis and biological activities

Wei, Yan,Li, Shi-qiang,Hao, Shuang-hong

, p. 1824 - 1831 (2017/11/28)

Twelve angular oxazole-fused coumarin derivatives were designed, synthesised and characterised by 1H NMR, 13C NMR and HRMS. The structure of compound 4a was further confirmed by X-ray single-crystal diffraction. The bioassay experiment results indicated that compounds 4f and 4l have high antifungal activity on the mycelium growth of 4 plant disease fungi. Especially, compound 4l has a stronger antifungal activity compare to the commercial fungicide, Carbendazim. The herbicidal activity experiment showed that 4a and 4b can significantly inhibit the taproot and caulis development of Chenopodium album seedling and have better activities than the commercial herbicide, Acetochlor.

Synthesis of Fused Oxazolocoumarins from o-Hydroxynitrocoumarins and Benzyl Alcohol Under Gold Nanoparticles or FeCl3 Catalysis

Vlachou, Evangelia-Eirini N.,Armatas, Gerasimos S.,Litinas, Konstantinos E.

, p. 2447 - 2453 (2017/07/25)

Synthesis of fused oxazolocoumarins has been achieved from the one-pot tandem reactions of o-hydroxynitrocoumarins with benzyl alcohol in toluene under catalysis in a sealed tube at 150°C. The catalysis was performed by gold nanoparticles supported on TiO

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