51234-92-5 Usage
General Description
α-Methyl-2-(4-nitrophenyl)-5-benzoxazoleacetic acid is a chemical compound that belongs to the class of benzoxazoleacetic acids. It is characterized by the presence of a methyl group at the alpha position, a nitrophenyl group at the 2-position, and a benzoxazole ring at the 5-position. α-Methyl-2-(4-nitrophenyl)-5-benzoxazoleacetic acid is often used in pharmaceutical research and drug development due to its potential biological activities. Its molecular structure and properties make it a valuable target for the synthesis of new drugs and pharmacological agents. Additionally, α-Methyl-2-(4-nitrophenyl)-5-benzoxazoleacetic acid may have applications in the field of medicinal chemistry and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 51234-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51234-92:
(7*5)+(6*1)+(5*2)+(4*3)+(3*4)+(2*9)+(1*2)=95
95 % 10 = 5
So 51234-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H12N2O5/c1-9(16(19)20)11-4-7-14-13(8-11)17-15(23-14)10-2-5-12(6-3-10)18(21)22/h2-9H,1H3,(H,19,20)
51234-92-5Relevant articles and documents
Benzoxazole derivatives in treating inflammation, pain and fever
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, (2008/06/13)
The invention provides novel 5- and 6-benzoxazolyl alkanoic acids, optionally substituted in the 2-position, and derivatives thereof which possess anti-inflammatory, anti-pyretic and analgesic activity. Also provided is a process for preparing such compounds by cyclising an appropriately substituted o-aminophenol and, if necessary, converting the resultant benzoxazole to the desired compound.