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Benzaldehyde (5-anilino-[1,3,4]thiadiazol-2-yl)-hydrazone is a complex organic compound with the chemical formula C14H12N4OS. It is a derivative of benzaldehyde, featuring a hydrazone functional group and a 5-anilino-[1,3,4]thiadiazol-2-yl moiety. benzaldehyde (5-anilino-[1,3,4]thiadiazol-2-yl)-hydrazone is characterized by its unique structure, which includes a benzene ring, an aldehyde group, a hydrazone linkage, and a thiadiazole ring with an aniline substituent. It is synthesized through a condensation reaction between benzaldehyde and 5-aminothiadiazol-2-amine, followed by the formation of the hydrazone group. Benzaldehyde (5-anilino-[1,3,4]thiadiazol-2-yl)-hydrazone has potential applications in the field of pharmaceuticals and materials science, particularly as a precursor for the synthesis of various heterocyclic compounds with potential biological activities. Its chemical properties and reactivity make it a subject of interest for researchers exploring new synthetic routes and applications in organic chemistry.

5319-84-6

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5319-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5319-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5319-84:
(6*5)+(5*3)+(4*1)+(3*9)+(2*8)+(1*4)=96
96 % 10 = 6
So 5319-84-6 is a valid CAS Registry Number.

5319-84-6Downstream Products

5319-84-6Relevant academic research and scientific papers

Synthesis of 2′-(substituted)benzylidene hydrazino-5-arylamino-1,3,4- thiadiazoles and their antimicrobial activity

Burghate, Megha K.,Gandhe, Shital V.,Ajmire,Berad

, p. 103 - 108 (2008/03/11)

Several 2′-(substituted)benzylidene hydrazino-5-arylamino-1,3,4- thiadiazoles (5a-m) have been synthesized by the condensation of 1-(N-aryl thioamido)thiocarbohydrazides (3a-f) and different aromatic aldehydes in benzene medium, followed by intramolecular cyclization of compounds (4a-m) in refluxing ethanol medium. The former in turn have been prepared by the reaction of aryl isothiocynates (2a-f) and thiocarbohydrazide (1). Compounds (5a-m) on bromination with bromine in glacial acetic acid afforded dibromo derivatives (6a-m). The synthesized compounds were assayed for their antimicrobial activity against gram positive as well as gram negative micro-organisms.

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