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1-ETHYL-4-[(4-METHYLPHENYL)SULFONYL]-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 282109-01-7 Structure
  • Basic information

    1. Product Name: 1-ETHYL-4-[(4-METHYLPHENYL)SULFONYL]-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE
    2. Synonyms: 1-ETHYL-4-[(4-METHYLPHENYL)SULFONYL]-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE;1-ethyl-4-(4-methylbenzenesulfonyl)-2,3-dihydro-1H-imidazol-2-one
    3. CAS NO:282109-01-7
    4. Molecular Formula: C12H14N2O3S
    5. Molecular Weight: 266.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 282109-01-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-ETHYL-4-[(4-METHYLPHENYL)SULFONYL]-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-ETHYL-4-[(4-METHYLPHENYL)SULFONYL]-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE(282109-01-7)
    11. EPA Substance Registry System: 1-ETHYL-4-[(4-METHYLPHENYL)SULFONYL]-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE(282109-01-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 282109-01-7(Hazardous Substances Data)

282109-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 282109-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,2,1,0 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 282109-01:
(8*2)+(7*8)+(6*2)+(5*1)+(4*0)+(3*9)+(2*0)+(1*1)=117
117 % 10 = 7
So 282109-01-7 is a valid CAS Registry Number.

282109-01-7Downstream Products

282109-01-7Relevant articles and documents

Solid-phase synthesis of disubstituted 1,3-dihydro-2H-imidazol-2-ones

Patek,Weichsel,Drake,Smrcina

, p. 1322 - 1324 (2005)

An efficient and straightforward solid-phase synthesis of sulfonylimidazolones 2a-g is described. Our design was directed toward obtaining molecules for a general library development and incorporates functionalities that fulfill lead-like criteria. The synthesis was realized with the use of SPOS in fair to good yields and purity. Monitoring and quantitation of intermediates and final products were performed by the use of LCMS and NMR spectroscopy.

The reaction of 1,2-diones with ureas - A synthesis of 4-(1-substituted)alkylimidazol-2-ones

Liepa, Andris J.,Wright, Denis M.J.

, p. 73 - 76 (2007/10/03)

The reaction between glyoxal and ureas or thioureas in formic acid in the presence of sulfmates gives 4-arylsulfonylimidazol-2-ones such as (3b) and (3e). Labile 4-arylsulfonyl-5-hydroxyimidazolidin-2-ones (2a-c) may be isolated. Acyclic or cyclic 1,2-diketones react with ureas in the presence of selected nucleophiles to give side-chain substituted imidazol-2-ones (5a-e). CSIRO 2000.

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