6345-57-9 Usage
Uses
Used in Organic Synthesis:
[(carbamoylamino)-(2-hydroxyphenyl)methyl]urea is used as a reagent in organic synthesis for [application reason] the creation of various organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of complex molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [(carbamoylamino)-(2-hydroxyphenyl)methyl]urea is used as a pharmaceutical intermediate for [application reason] the development of new drugs and therapeutic agents. Its potential applications in this area are currently being studied and explored.
Used in Agricultural Applications:
[(carbamoylamino)-(2-hydroxyphenyl)methyl]urea may also be used in agricultural applications as [application type] a chemical with potential uses in crop protection or enhancement, for [application reason] its reactivity and functional groups that can be tailored to specific needs in agriculture.
Used in Industrial Applications:
Furthermore, [(carbamoylamino)-(2-hydroxyphenyl)methyl]urea has potential uses in industrial applications, where it can be utilized as [application type] a building block or intermediate for the production of various industrial chemicals, for [application reason] its versatility and reactivity in chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 6345-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6345-57:
(6*6)+(5*3)+(4*4)+(3*5)+(2*5)+(1*7)=99
99 % 10 = 9
So 6345-57-9 is a valid CAS Registry Number.
6345-57-9Relevant academic research and scientific papers
An investigation leading to preparation of tetrahydro-quinazoline derivatives involving ureidoalkylation and α-amidoalkylation reactions
Pandey,Mukesh,Kumar, Anilesh,Trivedi, Noopur
experimental part, p. 1910 - 1914 (2009/05/30)
Reaction of an aldehyde with excess equivalent of urea in ethanol affords alkylideno/arylideno-bis-ureas 1 which on condensation with p-aminophenol in acidic medium cyclised to 4-aralkyl-6-hydroxy-2-oxo-1,2,3,4- tetrahydroquinazolines 2. Reaction of 2 with arylamidoalcohols in concentrated H2SO4 results in 4-arylkyl-7-arylamido/imidoalkyl-6- hydroxy-2-oxo-1,2,3,4-tetrahydroquinazolines 3, Compounds 3 have been evaluated for their effect on central nervous system (CNS) and cardiovascular system (CVS).
