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6-(4-bromophenyl)-3-(4-methylphenyl)-7H-thiazolo[3,2-b][1,2,4]triazin-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1258875-45-4

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1258875-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258875-45-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,8,7 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1258875-45:
(9*1)+(8*2)+(7*5)+(6*8)+(5*8)+(4*7)+(3*5)+(2*4)+(1*5)=204
204 % 10 = 4
So 1258875-45-4 is a valid CAS Registry Number.

1258875-45-4Downstream Products

1258875-45-4Relevant academic research and scientific papers

Synthesis and biological evaluation of 3,6-diaryl-7H-thiazolo[3,2-b] [1,2,4]triazin-7-one derivatives as acetylcholinesterase inhibitors

Jin, Zhe,Yang, Liu,Liu, Si-Jie,Wang, Jian,Li, Shuo,Lin, Huang-Quan,Wan, David Chi Cheong,Hu, Chun

, p. 1641 - 1649 (2010)

Acetylcholinesterase (AChE) inhibitors played an important role in developing a cure for Alzheimer' s disease. In order to study on the influence of modifications at different groups and side chains on the AChE inhibitory ability and the active sites of 7

Thiazole[3,2-b]-1,2,4-thiazole derivatives and application thereof

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Paragraph 0114; 0119; 0120; 0133; 0134, (2018/02/04)

The invention belongs to the technical field of medicine and relates to thiazole[3,2-b]-1,2,4-thiazole derivatives and an application thereof. The thiazole[3,2-b]-1,2,4-thiazole derivatives comprise thiazole[3,2-b]-1,2,4-thiazole derivative compounds as well as stereoisomers and pharmaceutically applicable salts of the compounds, and a general structural formula of the compounds is represented in the specification; the thiazole[3,2-b]-1,2,4-thiazole derivatives and the pharmaceutically applicable acid-addition salts of the compounds can be combined with existing drugs or separately utilized to serve as glucose concentration dependent type insulin secretion accelerants for treatment of type II diabetes. Compared with the prior art, the compounds are the glucose concentration dependent type insulin secretion accelerants, can promote insulin secretion under high glucose concentration and do not influence insulin secretion under low glucose concentration, so that the side effect of hypoglycemia is avoided.

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