108857-45-0 Usage
Uses
Used in Organic Synthesis:
1-(3-NITROPHENYL)IMIDAZOLIDIN-2-ONE is used as a building block for the synthesis of various organic compounds, leveraging its unique structure and reactivity to create a wide array of molecules.
Used in Pharmaceutical Research:
1-(3-NITROPHENYL)IMIDAZOLIDIN-2-ONE is used as a precursor in the development of new drugs, taking advantage of its functional groups to design and synthesize pharmaceutically active molecules.
Used in Agrochemical Development:
1-(3-NITROPHENYL)IMIDAZOLIDIN-2-ONE is used as a starting material in the creation of agrochemicals, with its potential to form new compounds that can be applied in agriculture for pest control and crop protection.
Used in Chemical Research:
1-(3-NITROPHENYL)IMIDAZOLIDIN-2-ONE is utilized in research to explore its reactivity and properties, contributing to the understanding of chemical reactions and the development of new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 108857-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,5 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108857-45:
(8*1)+(7*0)+(6*8)+(5*8)+(4*5)+(3*7)+(2*4)+(1*5)=150
150 % 10 = 0
So 108857-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O3/c13-9-10-4-5-11(9)7-2-1-3-8(6-7)12(14)15/h1-3,6H,4-5H2,(H,10,13)
108857-45-0Relevant articles and documents
SULFONAMIDE DERIVATIVE AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALT THEREOF
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Paragraph 0782-0783, (2018/07/15)
The present invention aims to provide a novel low-molecular-weight compound exhibiting an orexin receptor agonist activity and expected to be useful as a prophylactic or therapeutic agent for narcolepsy and the like. The present invention provides a compo
Preparation of N-substituted imidazolidinones and N-substituted 2-thionimidazolidinones
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, (2008/06/13)
The invention is a process for the preparation of N-substituted imidazolidinones and N-substituted 2-thionimidazolidinones which comprises contacting an oxazolidinone with a compound containing a nitrogen directly bonded to a carbonyl or a thiocarbonyl group in the presence of a Lewis acid catalyst or the hydrate of a Lewis acid catalyst under conditions such that an N-substituted imidazolidinone or N-substituted 2-thionimidazolidinone is prepared. The compound containing a nitrogen directly bonded to a carbonyl or a thiocarbonyl group is an isocyanate or isothiocyanate or a compound wherein the nitrogen is reactive and the carbonyl or thiocarbonyl group is further bonded to a substituent by a bond which is clevable under the reaction conditions. The Lewis acid catalyst corresponds to the formula wherein M is a group IB-VIIIB, IIIA or IVA element with the proviso that M is not C or Si; X is a halogen; and n is 2, 3 or 4.