104662-85-3 Usage
Uses
Used in Pharmaceutical Industry:
METHYL(6-METHYL-2H-1,4-BENZOXAZIN-3(4H)-ONE-2-YL)ACETATE is used as a pharmaceutical compound for its potential biological activities. Its unique structure may contribute to the development of new drugs or therapeutic agents, particularly in the areas of disease treatment and prevention.
Used in Agricultural Industry:
In agriculture, METHYL(6-METHYL-2H-1,4-BENZOXAZIN-3(4H)-ONE-2-YL)ACETATE may be utilized as a bioactive agent with potential applications in pest control, crop protection, or as a component in the development of environmentally friendly agrochemicals.
Used in Materials Science:
METHYL(6-METHYL-2H-1,4-BENZOXAZIN-3(4H)-ONE-2-YL)ACETATE's unique molecular structure may also find applications in materials science, where it could be employed in the synthesis of new materials with specific properties, such as high-performance polymers or advanced composites.
Further research into the properties and applications of METHYL(6-METHYL-2H-1,4-BENZOXAZIN-3(4H)-ONE-2-YL)ACETATE is necessary to fully explore its potential and unlock its capabilities across various industries.
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 academic research and scientific papers
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.
