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[6-(4-Methoxy-phenyl)-3-phenyl-imidazo[2,1-b]thiazol-2-yl]-acetic acid is a complex organic compound with the molecular formula C21H17N3O2S. It features a 2-imidazo[2,1-b]thiazolyl core, which is a heterocyclic ring system consisting of an imidazole fused to a thiazole. The compound has a 4-methoxy-phenyl group attached at position 6, which introduces a methoxy substituent that can influence its electronic properties and solubility. Additionally, a phenyl group is attached at position 3, further contributing to the compound's structure and potential biological activity. This chemical is known for its potential applications in pharmaceutical research, particularly as a building block for the development of new drugs, due to its unique structure and the possibility of forming various interactions with biological targets.

81950-03-0

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81950-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81950-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,5 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81950-03:
(7*8)+(6*1)+(5*9)+(4*5)+(3*0)+(2*0)+(1*3)=130
130 % 10 = 0
So 81950-03-0 is a valid CAS Registry Number.

81950-03-0Downstream Products

81950-03-0Relevant academic research and scientific papers

Synthesis and Anthiinflammatory Activity of Some Arylimidazothiazolyl- and Arylimidazobenzothiazolyl-acetic Acids

Sawhney, S. N.,Kodali, Dharma R.,Dhindsa, G. S.,Singh, S. P.

, p. 134 - 138 (2007/10/02)

Three series of the title compounds, imidazothiazolyl-, imidazobenzothiazolyl- and imidazobenzothiazolylaryl-acetic acids (II,III and IV) have been synthesised for evaluation as potential anti-inflammatory agents.Compounds II have been synthesised by condensing ethyl (2-amino-4-aryl-5-thiazolyl)acetate (VI) with phenacyl bromides followed by hydrolysis of the resultant esters (VII).III are obtained by the condensatiion of ethyl 2-aminobenzothiazole-6-acetate with phenacyl bromides followed by hydrolysis of the resultant esters (IX).Compound IV result from the treatment of 2-aminobenzothiazoles with ethyl 4(ω-bromoacetylphenyl)acetate (XI) followed by hydrolysis of the esters (XII).Some of the title compounds show good antiinflammatory activity.

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