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[1,3]dithiolan-2-ylidene-(5-p-tolyl-[1,3,4]oxadiazol-2-yl)-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

201343-18-2

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201343-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201343-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,3,4 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 201343-18:
(8*2)+(7*0)+(6*1)+(5*3)+(4*4)+(3*3)+(2*1)+(1*8)=72
72 % 10 = 2
So 201343-18-2 is a valid CAS Registry Number.

201343-18-2Downstream Products

201343-18-2Relevant academic research and scientific papers

Spiro-heterocycles containing 1,3,4-oxadiazole: A convenient synthesis of 3-(5- Substitutedphenyl-l,3,4-oxadiazole-2-yl)-5,8-dithiaspiro[3,4]-octan-2-onesand 1,4-dithia-6-azaspiro[4,4]-nonan-7-ones

Tiwari, Shailendra,Singh, Kamal Pratap,Pathak, Poonam,Ahmad, Akeel

, p. 1060 - 1064 (2019/05/22)

A new series of novel 3-(5-substituted phenyl-l,3,4-oxadiazole-2-yl)-5,8-dithiaspiro [3,4]-octan-2-ones and l,4-dithia-6- azaspiro[4,4]nonan-7-ones have been synthesized from a common intermediate, in good yields. These compounds have been screened for th

Synthesis of 5-aryl-2-[spiro-(1,3-dithiolane)-2,4'-(3'-chloro-2'-azetidinon)-1'-yl]-1,3,4-oxa(thia)diazoles and 5-aryl-2-[spiro-(1,3-dithiolane)-2,2'-(4'-thiazolidinon)-3'-yl]-1,3,4-oxa(thia)diazoles as antimicrobial agents

Khan, Mukhtar Hussain,Nizamuddin

, p. 625 - 629 (2007/10/03)

5-Aryl-2-[spiro-(1,3-dithiolane)-2,4'-(3'-chloro-2'-azetidinon)-1'-yl]-1,3,4-oxa(thia)diazoles 4 and 5-aryl-2-[spiro-(1,3-dithiolane)-2,2'-(4'-thiazolidinon)-3'-yl]-1,3,4-oxa(thia)diazoles 5 have been synthesised from 5-aryl-2-(1,3-dithiolan-2-yl)imino-1,3,4-oxa(thia)diazoles 3 with chloro acetyl chloride and mercapto acetic acid, respectively. These compounds have been screened on Aspergillus niger, Pyricularia oryzae, Fusarium oxysporum and Cephalosporum sacchari; and Escherichia coli, Salmonella typhi and Bacillus aureus for their antifungal and antibacterial activities, respectively.

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