53414-34-9 Usage
Urea derivative
A compound derived from urea (a molecule containing two amine groups attached to a carbonyl group) with structural modifications.
Methyl substituent
A small alkyl group (a carbon atom bonded to three hydrogen atoms) attached to the urea derivative, influencing the compound's properties and reactivity.
Building block in organic synthesis
1-methyl-3-(2-nitrophenyl)urea is used as a starting material or intermediate in the synthesis of more complex organic compounds.
Pharmaceutical research
The compound is studied for its potential applications in the development of new drugs due to its unique structure and properties.
Antimicrobial properties
1-methyl-3-(2-nitrophenyl)urea has been shown to exhibit activity against microorganisms, such as bacteria and fungi, making it a potential candidate for antimicrobial drug development.
Anti-inflammatory properties
The compound may help reduce inflammation, a response to injury or infection in the body, which is a common target for many medications.
Pesticide or herbicide application
1-methyl-3-(2-nitrophenyl)urea has been shown to inhibit the growth of certain plant species, suggesting its potential use as a pesticide or herbicide in agriculture.
Importance in various fields
The compound's unique structure and properties make it an important building block in fields such as medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 53414-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,1 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53414-34:
(7*5)+(6*3)+(5*4)+(4*1)+(3*4)+(2*3)+(1*4)=99
99 % 10 = 9
So 53414-34-9 is a valid CAS Registry Number.
53414-34-9Relevant articles and documents
Synthesis of Bi- and Tri-cyclic Tetrazepinones
Bertrand, J. Jean-Claude,Just, George
, p. 2525 - 2529 (2007/10/02)
Diazotization of N,N'-dialkyl-N-(o-aminophenyl) ureas 7, 13 and 17 gave 3,5-dimethyl-3H-1,2,3,5-benzotetrazepin-4(5H)-one 8, 3-methyl-6,7-dihydro-1,2,3,5-tetrazepinoquinolin-4(3H)-one 14 and 3-methyl-6,7-dihydrooxazino-1,2,3,5-benzotetrazepin-4-one 19.The structures of these bi- and tri-cyclic systems were confirmed by 1H, 13C and 15N NMR data.X-Ray diffraction of compound 14 shows that the tetrazepinone ring is nonplanar.
