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4-(4-fluoro-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 221121-43-3 Structure
  • Basic information

    1. Product Name: 4-(4-fluoro-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester
    2. Synonyms: 4-(4-fluoro-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester
    3. CAS NO:221121-43-3
    4. Molecular Formula:
    5. Molecular Weight: 238.259
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 221121-43-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(4-fluoro-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-fluoro-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester(221121-43-3)
    11. EPA Substance Registry System: 4-(4-fluoro-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester(221121-43-3)
  • 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: 221121-43-3(Hazardous Substances Data)

221121-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221121-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,2 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 221121-43:
(8*2)+(7*2)+(6*1)+(5*1)+(4*2)+(3*1)+(2*4)+(1*3)=63
63 % 10 = 3
So 221121-43-3 is a valid CAS Registry Number.

221121-43-3Relevant articles and documents

Synthesis and biological evaluation of novel anti-hepatitis C virus (HCV) agents: 2-hydroxylphenethyl sulfanyl-oxopyrimidines

Wu, Daochun,Feng, Yue,Wang, Hua,Yang, Junfeng,Chen, Xian,Wang, Yueping,Cong Lai, Christopher,Zhang, Yufang,Li, Cong,Xia, Xueshan,He, Yanping

, p. 1388 - 1396 (2017/06/05)

A novel series of dihydro-hydroxyl-phene-thylsulfanyl-ω-cyclohexyl/phenyl-oxopyrimidine derivatives have been synthesized and their in vitro anti-hepatitis C virus activities have been evaluated using Huh 7.5.1 cells. Some of the compounds showed moderate

Solution-phase parallel synthesis of S-DABO analogues

Togninelli, Andrea,Carmi, Caterina,Petricci, Elena,Mugnaini, Claudia,Massa, Silvio,Corelli, Federico,Botta, Maurizio

, p. 65 - 67 (2007/10/03)

A simple and straightforward methodology for the parallel, solution-phase synthesis of a new series of S-DABO derivatives 1 and 2, bearing aromatic substituents at the C2 and C6 positions, has been developed. Starting from potassium ethyl malonates 3, thi

Parallel solution-phase and microwave-assisted synthesis of new S-DABO derivatives endowed with subnanomolar anti-HIV-1 activity

Manetti, Fabrizio,Esté, José A.,Clotet-Codina, Imma,Armand-Ugón, Mercedes,Maga, Giovanni,Crespan, Emmanuele,Cancio, Reynel,Mugnaini, Claudia,Bernardini, Cesare,Togninelli, Andrea,Carmi, Caterina,Alongi, Maddalena,Petricci, Elena,Massa, Silvio,Corelli, Federico,Botta, Maurizio

, p. 8000 - 8008 (2007/10/03)

A simple and efficient methodology for the parallel solution-phase synthesis has been set up to obtain a series of thiouracils, in turn selectively S-benzylated under microwave irradiation to give new S-DABOs. Biological screening led to the identificatio

5-alkyl-2-(alkylthio)-6-(2,6-dihalophenylmethyl)-3,4-dihydropyrimidin- 4(3H)-ones: Novel potent and selective dihydro-alkoxy-benzyl-oxopyrimidine derivatives

Mai, Antonello,Artico, Marino,Sbardella, Gianluca,Massa, Silvio,Novellino, Ettore,Greco, Giovanni,Loi, Anna Giulia,Tramontano, Enzo,Marongiu, Maria Elena,La Colla, Paolo

, p. 619 - 627 (2007/10/03)

Molecular modeling analysis of compounds belonging to the recently published series of dihydro-alkoxy-benzyl-oxopyrimidines (DABOs), such as S- DABOs and DATNOs, gave support to the design of new 2,6-disubstituted benzyl- DABO derivatives as highly potent

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