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benzyl-[5-(4-methoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23282-99-7

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23282-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23282-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,8 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23282-99:
(7*2)+(6*3)+(5*2)+(4*8)+(3*2)+(2*9)+(1*9)=107
107 % 10 = 7
So 23282-99-7 is a valid CAS Registry Number.

23282-99-7Downstream Products

23282-99-7Relevant 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-

Versatile strategies for the solid phase synthesis of small heterocyclic scaffolds: [1,3,4]-Thiadiazoles and [1,3,4]-oxadiazoles

Severinsen, Rune,Kilburn, John Paul,Lau, Jesper F.

, p. 5565 - 5575 (2007/10/03)

New robust protocols for the solid phase synthesis of 5-alkylthio-, 5-alkyl/aryl-, and 5-acylamino-2-alkylamino-[1,3,4]-thiadiazoles are described based on a common resin bound thiosemicarbazide. A protocol for the solid phase synthesis of 2-alkyl/aryl-amino-5-alkylamino-[1,3,4]-oxadiazoles from a resin bound semicarbazide is likewise reported. The protocols have been verified by the preparation of four small libraries that all gave products in good to excellent yields and purity.

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