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2-(thien-2-yl)-5-phenyl-1,3,4-thiadiazole is a heterocyclic compound characterized by the presence of a thiadiazole ring, which is a five-membered ring containing two nitrogen atoms and one sulfur atom. The molecule features a phenyl group attached to the 5-position of the thiadiazole ring and a thien-2-yl group (a thiophene ring with a hydrogen atom at the 2-position) attached to the 2-position. This chemical structure is of interest in the field of organic chemistry and material science, as it can be used in the synthesis of various compounds with potential applications in pharmaceuticals, agrochemicals, and other industries. The specific properties and reactivity of 2-(thien-2-yl)-5-phenyl-1,3,4-thiadiazole depend on the electronic and steric effects of the substituents, making it a versatile building block for the development of new molecules with tailored properties.

1456-73-1

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1456-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1456-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,5 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1456-73:
(6*1)+(5*4)+(4*5)+(3*6)+(2*7)+(1*3)=81
81 % 10 = 1
So 1456-73-1 is a valid CAS Registry Number.

1456-73-1Downstream Products

1456-73-1Relevant academic research and scientific papers

HETEROCYCLIZATION OF DERIVATIVES OF THIONCARBOXYLIC ACIDS TO 1,3,4-THIADIAZOLES UNDER THE ACTION OF TERT-BUTYL HYPOCHLORITE

Demchuk, D. V.,Lutsenko, A. I.,Troyanskii, E. I.,Nikishin, G. I.

, p. 1690 - 1695 (1989)

A method for synthesis of 2-alkyl-5-aryl- and 2,5-diaryl-1,3,4-thiadiazoles by successive reaction of thioamides with tert-butyl hypochlorite and benzothiohydrazides was developed.The first step in the formation of 1,3,4-thiadiazoles consists of oxidation

Greener and rapid access to bio-active heterocycles: one-pot solvent-free synthesis of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles

Polshettiwar, Vivek,Varma, Rajender S.

, p. 879 - 883 (2008/09/17)

A novel one-pot solvent-free synthesis of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles by condensation of acid hydrazide and triethyl orthoalkanates under microwave irradiations is reported. This green protocol was catalyzed efficiently by solid supported NafionNR50 and phosphorus pentasulfide in alumina (P4S10/Al2O3) with excellent yields.

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