104662-85-3 Usage
General Description
METHYL(6-METHYL-2H-1,4-BENZOXAZIN-3(4H)-ONE-2-YL)ACETATE is a chemical compound with a molecular structure containing a benzoxazinone ring and a methyl acetate group. It is a derivative of 6-methyl-2H-1,4-benzoxazin-3(4H)-one, a natural compound found in various plant species that is known for its potential biological activities. METHYL(6-METHYL-2H-1,4-BENZOXAZIN-3(4H)-ONE-2-YL)ACETATE may have uses in the fields of pharmaceuticals, agriculture, and materials science due to its unique structure and potential functional properties. Further research into its properties and applications may reveal its potential for various industrial and scientific uses.
Check Digit Verification of cas no
The CAS Registry Mumber 104662-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,6 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104662-85:
(8*1)+(7*0)+(6*4)+(5*6)+(4*6)+(3*2)+(2*8)+(1*5)=113
113 % 10 = 3
So 104662-85-3 is a valid CAS Registry Number.
104662-85-3Relevant articles and documents
A Convenient and One-Pot Synthesis of Methyl &α-(3,4-Dihydro-3-oxo-2H-1,4-benzoxazin-2-yl)acetates
Shridhar, S. R.,Ram, Bhagat,Rao, K. Srinivasa,Jain, M. L.
, p. 992 - 994 (2007/10/02)
A convenient and one-step method for the preparation of methyl α-(6-substituted 3,4-dihydro-3-oxo-2H-1,4-benzoxazin-2-yl)acetates (1a, and 8-14) is described.The reaction of appropriately substituted 2-aminophenols with maleic anhydride in the presence of Et3N gives the corresponding benzoxazinylacetates (1a and 8-10) while with methylmaleic anhydride, an initial nucleophilic attack at the more hindered carbonyl group takes place leading to the formation of the corresponding 2-methylbenzoxazinylacetates (11-14) in excellent yields.The antiinflammatory activity of these acetates (1a and 8-14) is also described.