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2-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazole is a chemical compound with the molecular formula C10H11N2O5. It is a derivative of the 1,3,4-oxadiazole heterocycle, which is characterized by a five-membered ring containing two nitrogen atoms and one oxygen atom. In this specific compound, the oxadiazole ring is substituted with a 3,4,5-trimethoxyphenyl group, which consists of a benzene ring with three methoxy groups attached at the 3rd, 4th, and 5th carbon positions. 2-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazole is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique chemical structure and properties.

5378-26-7

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5378-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5378-26-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5378-26:
(6*5)+(5*3)+(4*7)+(3*8)+(2*2)+(1*6)=107
107 % 10 = 7
So 5378-26-7 is a valid CAS Registry Number.

5378-26-7Relevant articles and documents

Spectral-Luminescent Properties of 2-Aryl-1,3,4-oxadiazoles

Mikhailov,Artyushkina, Yu. M.,Dushenko,Mikhailova,Revinskii, Yu. V.,Minkin

, p. 602 - 604 (2018)

Refluxing equimolar amounts of acylhydrazides with triethyl orthoformate in o-xylene yielded 2-aryl-1,3,4-oxadiazoles luminescing with high quantum yields in polar and nonpolar solvents (λm fl ax 299–349 nm, φ 0.20–0.62). The only exception was 2-(1,3,4-o

Copper-catalyzed direct cross coupling of 1,3,4-oxadiazoles with trans-β-halostyrenes: Synthesis of 2-E-vinyl 1,3,4-oxadiazoles

Das, Biswanath,Reddy, Gandolla Chinna,Balasubramanyam, Penagaluri,Salvanna

supporting information; experimental part, p. 300 - 305 (2012/01/05)

The first direct C-H alkenylation of 1,3,4-oxadiazoles with trans-β-halo olefinic system has been carried out using a combination of CuI/DMEDA as a catalyst. A wide range of 2-E-vinyl-substituted oxadiazoles were obtained in high yields (85-93%).

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