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[6-Biphenyl-4-yl-3-(4-chloro-phenyl)-imidazo[2,1-b]thiazol-2-yl]-acetic acid ethyl ester is a complex organic compound with the molecular formula C27H20ClN3O2S. It is characterized by a biphenyl-4-yl group attached to the imidazo[2,1-b]thiazol-2-yl core, with a 4-chloro-phenyl substituent at position 3. The molecule features an acetic acid ethyl ester functional group, which is an ester derived from acetic acid and ethanol. [6-Biphenyl-4-yl-3-(4-chloro-phenyl)-imidazo[2,1-b]thiazol-2-yl]-acetic acid ethyl ester is known for its potential applications in medicinal chemistry, particularly as a precursor or intermediate in the synthesis of biologically active molecules. Its structure and properties make it a candidate for further exploration in drug development, given its ability to form stable complexes with various biological targets.

81950-47-2

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81950-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81950-47-2 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, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81950-47:
(7*8)+(6*1)+(5*9)+(4*5)+(3*0)+(2*4)+(1*7)=142
142 % 10 = 2
So 81950-47-2 is a valid CAS Registry Number.

81950-47-2Relevant 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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