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1,2-bis(4-amino-5-phenyl-1,2,4-triazole-3-yl-sulfanylmethyl)quinoxaline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

436849-73-9

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436849-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 436849-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,8,4 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 436849-73:
(8*4)+(7*3)+(6*6)+(5*8)+(4*4)+(3*9)+(2*7)+(1*3)=189
189 % 10 = 9
So 436849-73-9 is a valid CAS Registry Number.

436849-73-9Downstream Products

436849-73-9Relevant academic research and scientific papers

Anionic ligands tune the structural and catalytic properties of quinoxaline-based copper(II) complexes as mimetics of copper-containing oxidase protein

Fathy, Ahmed M.,Hessien, Mahmoud M.,Ibrahim, Mohamed M.,Ramadan, Abd El-Motaleb M.

, (2021/11/17)

The hexadentate ligand containing quinoxaline backbone along with its Cu(II) -based complexes with various anionic ligands were synthesized and their structures were determined. Molecular formulae were assigned based on the data of both elemental analysis

Unexpected synthesis of novel condensed heteromacrocycles

Elwahy, Ahmed H. M.,Abbas, Ashraf A.,Kassab, Refaie M.

, p. 260 - 264 (2007/10/03)

Alkylation of 4-amino-1,2,4-triazol-3(2H)-thiones 9a-d with 2,3-bis(bromomethyl)quinoxaline (8) in absolute ethanol containing potassium hydroxide gave the corresponding bis(amines) 10a-d. Condensation of the latter with the apprbpriate aromatic aldehydes in refluxing acetic acid afforded the corresponding benzylideneamino derivatives 12a,b. On the other hand, reaction of the bis(amines) 10a-d with the bis(aldehydes) 13a-c in refluxing acetic acid under high dilution conditions did not lead to the formation of the corresponding macrocyclic Schiffs bases 14. Instead, the reaction gave the corresponding novel condensed heteromacrocycles 15a-f.

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