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

23343-95-5

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23343-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23343-95-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,4 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23343-95:
(7*2)+(6*3)+(5*3)+(4*4)+(3*3)+(2*9)+(1*5)=95
95 % 10 = 5
So 23343-95-5 is a valid CAS Registry Number.

23343-95-5Downstream Products

23343-95-5Relevant 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

A Highly Efficient Diversification of 2-Amino/Amido-1,3,4-oxadiazole and 1,3,4-Thiadiazole Derivatives via Reagent-Based Cyclization of Thiosemicarbazide Intermediate on Solid-Phase

Yang, Seung-Ju,Choe, Ji-Hye,Abdildinova, Aizhan,Gong, Young-Dae

, p. 732 - 741 (2015/12/23)

A 2-amino/amido-1,3,4-oxadiazole and 1,3,4-thiadiazole library has been constructed on solid-phase organic synthesis. The key step on this solid-phase synthesis involves the preparation of polymer-bound 2-amino-1,3,4-oxadiazole and 1,3,4-thiadiazole core

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-

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