80589-72-6 Usage
Chemical compound
2-[4-(5-ethoxy-4-phenyl-1,3-oxazol-2-yl)phenyl]acetic acid
Structure
Consists of a phenyl group connected to a 1,3-oxazol-2-yl ring, further connected to an ethoxy group, and bound to an acetic acid group
Properties
Complex and unique structure, potential pharmacological properties
Applications
Interest in scientific research and drug development for its potential pharmacological properties
Further research needed
To fully understand its potential in various fields
Check Digit Verification of cas no
The CAS Registry Mumber 80589-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,8 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80589-72:
(7*8)+(6*0)+(5*5)+(4*8)+(3*9)+(2*7)+(1*2)=156
156 % 10 = 6
So 80589-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H17NO4/c1-2-23-19-17(14-6-4-3-5-7-14)20-18(24-19)15-10-8-13(9-11-15)12-16(21)22/h3-11H,2,12H2,1H3,(H,21,22)
80589-72-6Relevant academic research and scientific papers
Anti-Inflammatory Agents: Part V - Synthesis of Some New 4-(4,5-Disubstituted-oxazol-2-yl)phenylacetic Acids and their Methyl Esters
Shridhar, D. R.,Ram, Bhagat,Sarma, C. R.,Krishna, R. R.,Singh, P. P.,Rao, C. Seshagiri
, p. 891 - 893 (2007/10/02)
A series of 4-(4-aryl/alkyl-5-alkoxyoxazol-2-yl)phenylacetic acids (4a-j) has been synthesised by the reaction of appropriately substituted glycinate hydrochlorides (1a-j) with α-cyano-p-toluoyl chloride followed by cyclization and hydrolysis of the resulting N-α-cyano-p-toluoylglycinates (2a-j).Esterification (CH2N2) of the oxazolylphenylacetic acids (4a-g) furnishes the corresponding methyl esters (5a-g).Several compounds in this series show moderate anti-inflammatory activity at one fifth of their LD50 dose in the carrageenin-induced rat paw oedema test.
