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1,3,4-Thiadiazol-2-amine, N-(4-methoxyphenyl)-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63314-60-3

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63314-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63314-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63314-60:
(7*6)+(6*3)+(5*3)+(4*1)+(3*4)+(2*6)+(1*0)=103
103 % 10 = 3
So 63314-60-3 is a valid CAS Registry Number.

63314-60-3Downstream Products

63314-60-3Relevant academic research and scientific papers

Design and Synthesis of 1,3,4-Thiadiazole Derivatives as Novel Anticancer and Antitubercular Agents

Chandra Sekhar,Venkata Rao,Tejeswara Rao,Lav Kumar,Jha, Anjali

, p. 770 - 779 (2019/06/05)

A series of novel 5-phenyl-substituted 1,3,4-thiadiazole-2-amines were designed, synthesized, and screened for their antitumor and antitubercular activities. The target compounds were synthesized starting from isocyanates and acid hydrazides by convention

Regioselective synthesis of 2-amino-substituted 1,3,4-oxadiazole and 1,3,4-thiadiazole derivatives via reagent-based cyclization of thiosemicarbazide intermediate

Yang, Seung-Ju,Lee, Seok-Hyeong,Kwak, Hyun-Jung,Gong, Young-Dae

, p. 438 - 444 (2013/04/10)

A regioselective, reagent-based method for the cyclization reaction of 2-amino-1,3,4-oxadiazole and 2-amino-1,3,4-thiadiazole core skeletons is described. The thiosemicarbazide intermediate 3 was reacted with EDC·HCl in DMSO or p-TsCl, triethylamine in N-

The reactions of cyclization of thiosemicarbazide derivatives to 1,2,4-triazole or 1,3,4-thiadiazole system

Dobosz, Maria,Pitucha, Monika,Wujec, Monika

, p. 31 - 38 (2007/10/03)

In the reaction of hydrazide of formic, nicotinic and benzoic acid with isothiocyanates were obtained the respective thiosemicarbazide derivatives [I-XII]. Further cyclization with 2% NaOH solution led to formation of derivatives Δ2-1,2,4-triaz

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