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[6-(4-Chloro-phenyl)-3-(4-methoxy-phenyl)-imidazo[2,1-b]thiazol-2-yl]-acetic acid is a complex organic compound with the molecular formula C18H13ClN2O2S2. It is characterized by a unique structure that includes an imidazo[2,1-b]thiazole ring system, which is fused with a thiazole ring. The molecule features a 4-chlorophenyl group attached at position 6 and a 4-methoxyphenyl group at position 3, both of which are important for its chemical properties and potential applications. [6-(4-Chloro-phenyl)-3-(4-methoxy-phenyl)-imidazo[2,1-b]thiazol-2-yl]-acetic acid is known for its potential use in the development of pharmaceuticals, particularly as a kinase inhibitor, due to its ability to interact with specific protein targets in the body. The presence of the chlorine and methoxy groups contributes to its reactivity and selectivity, making it a subject of interest in medicinal chemistry and drug design.

81950-10-9

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81950-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81950-10-9 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, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81950-10:
(7*8)+(6*1)+(5*9)+(4*5)+(3*0)+(2*1)+(1*0)=129
129 % 10 = 9
So 81950-10-9 is a valid CAS Registry Number.

81950-10-9Downstream Products

81950-10-9Relevant 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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