Cas 81950-01-8,[6-(4-Fluoro-phenyl)-3-phenyl-imidazo[2,1-b]thiazol-2-yl]-acetic acid

81950-01-8

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Basic information

Product Name: [6-(4-Fluoro-phenyl)-3-phenyl-imidazo[2,1-b]thiazol-2-yl]-acetic acid
Synonyms: [6-(4-Fluoro-phenyl)-3-phenyl-imidazo[2,1-b]thiazol-2-yl]-acetic acid
CAS NO:81950-01-8
Molecular Formula:
Molecular Weight: 352.389
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [6-(4-Fluoro-phenyl)-3-phenyl-imidazo[2,1-b]thiazol-2-yl]-acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: [6-(4-Fluoro-phenyl)-3-phenyl-imidazo[2,1-b]thiazol-2-yl]-acetic acid(81950-01-8)
EPA Substance Registry System: [6-(4-Fluoro-phenyl)-3-phenyl-imidazo[2,1-b]thiazol-2-yl]-acetic acid(81950-01-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 81950-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81950-01-8 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 81950-01:
(7*8)+(6*1)+(5*9)+(4*5)+(3*0)+(2*0)+(1*1)=128
128 % 10 = 8
So 81950-01-8 is a valid CAS Registry Number.

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81950-01-8Relevant 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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