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(4-Oxo-5,6,7,8-tetrahydro-4H-benzo[4,5]thieno[2,3-d]pyrimidin-3-yl)-acetic acid is a complex organic compound that features a benzothieno pyrimidine ring system. As an acetic acid derivative, it has the chemical formula C14H14N2O3S. This molecule exhibits structural features commonly found in biologically active compounds, suggesting potential pharmaceutical applications.

40277-46-1

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40277-46-1 Usage

Uses

Used in Pharmaceutical Industry:
(4-Oxo-5,6,7,8-tetrahydro-4H-benzo[4,5]thieno[2,3-d]pyrimidin-3-yl)-acetic acid is used as a potential pharmaceutical agent due to its structural characteristics that are commonly found in biologically active molecules. Further research and analysis are necessary to fully understand its properties and potential uses in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 40277-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,7 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40277-46:
(7*4)+(6*0)+(5*2)+(4*7)+(3*7)+(2*4)+(1*6)=101
101 % 10 = 1
So 40277-46-1 is a valid CAS Registry Number.

40277-46-1Downstream Products

40277-46-1Relevant academic research and scientific papers

Synthesis, Antibacterial Activity, and Docking Studies of 1,2,3-triazole-tagged Thieno[2,3-d]pyrimidinone Derivatives

Aruna Kumari,Triloknadh,Harikrishna,Vijjulatha,Venkata Rao

, p. 3672 - 3681 (2017/11/21)

Novel (1-(substituted phenyl)-1H-1,2,3-triazol-4-yl)methyl-2-(4-oxo-5,6,7,8-tetrahydrobenzo[1,2]thieno[2,3-d]pyrimidin-3(4H)-yl)acetate derivatives were synthesized. All the compounds showed significant antibacterial activity against Gram-negative (Escherichia coli and Klebsiella pneumonia) and Gram-positive (Bacillus subtilis and Bacillus cereus) bacteria. Particularly, (1-(3-nitrophenyl)-1H-1,2,3-triazol-4-yl)methyl-2-(4-oxo-5,6,7,8-tetrahydrobenzo[1, 2]thieno[2,3-d]pyrimidin-3(4H)-yl)acetate was found to be most potent against E.?coli, K.?pneumonia, and B.?subtilis with MIC 25?μg/ml. Molecular docking was also performed on purine riboswitch of B.?subtilis and thiamine pyrophosphate riboswitch of E.?coli.

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