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[2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid is a complex organic compound derived from benzothiazole and aminobenzene, featuring a bromophenyl group and an imidazo ring system. This molecule possesses a carboxylic acid functional group, classifying it as a weak acid. It is widely recognized for its potential biological activities and is frequently utilized in pharmaceutical research and development. [2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid's unique structure and properties make it a promising candidate for various applications in medicinal chemistry, including the development of novel drugs and the study of biological processes. However, further research is required to fully comprehend its properties and potential uses.

81950-24-5

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81950-24-5 Usage

Uses

Used in Pharmaceutical Research and Development:
[2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid is used as a research compound for its potential biological activities. Its unique structure and properties make it a valuable tool in the development of new drugs and the study of various biological processes.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid is used as a chemical intermediate for the synthesis of novel drugs. Its unique structure and functional groups provide a foundation for the development of new therapeutic agents.
Used in Drug Design and Synthesis:
[2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid is employed as a key building block in drug design and synthesis. Its versatile structure allows for the creation of a wide range of drug candidates with potential applications in various therapeutic areas.
Used in Biological Research:
As a research tool, [2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid is used to study biological processes and mechanisms. Its unique properties and interactions with biological systems can provide valuable insights into the underlying processes and help identify potential therapeutic targets.
Used in Drug Discovery:
In the drug discovery process, [2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid is used as a starting material or a scaffold for the development of new drugs. Its structural diversity and potential biological activities make it an attractive candidate for the identification of novel therapeutic agents.
Used in Chemical Synthesis:
[2-(4-bromophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]acetic acid is utilized as a synthetic intermediate in the preparation of various chemical compounds. Its unique structure and functional groups enable the synthesis of a wide range of molecules with potential applications in different industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 81950-24-5 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, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81950-24:
(7*8)+(6*1)+(5*9)+(4*5)+(3*0)+(2*2)+(1*4)=135
135 % 10 = 5
So 81950-24-5 is a valid CAS Registry Number.

81950-24-5Downstream Products

81950-24-5Relevant 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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