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2-(2,4,5-trifluorophenyl)-2-oxazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1109138-88-6 Structure
  • Basic information

    1. Product Name: 2-(2,4,5-trifluorophenyl)-2-oxazoline
    2. Synonyms: 2-(2,4,5-trifluorophenyl)-2-oxazoline
    3. CAS NO:1109138-88-6
    4. Molecular Formula:
    5. Molecular Weight: 201.148
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1109138-88-6.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: 2-(2,4,5-trifluorophenyl)-2-oxazoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,4,5-trifluorophenyl)-2-oxazoline(1109138-88-6)
    11. EPA Substance Registry System: 2-(2,4,5-trifluorophenyl)-2-oxazoline(1109138-88-6)
  • 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: 1109138-88-6(Hazardous Substances Data)

1109138-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1109138-88-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,9,1,3 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1109138-88:
(9*1)+(8*1)+(7*0)+(6*9)+(5*1)+(4*3)+(3*8)+(2*8)+(1*8)=136
136 % 10 = 6
So 1109138-88-6 is a valid CAS Registry Number.

1109138-88-6Downstream Products

1109138-88-6Relevant articles and documents

Synthesis, microwave-assisted polymerization, and polymer properties of fluorinated 2-phenyl-2-oxazolines: A systematic study

Lobert, Matthias,Thijs, Hanneke M. L.,Erdmenger, Tina,Eckardt, Rebecca,Ulbricht, Christoph,Hoogenboom, Richard,Schubert, Ulrich S.

, p. 10396 - 10407 (2008)

We present a detailed systematic study of the synthesis and ability of fluorinated 2-phenyl-2-oxazolines to undergo polymerization. The synthesis of these compounds is based on a two-step procedure that gives the desired 2-oxazolines in moderate-to-good yields. All the compounds were fully characterized by IR and NMR (1H, 13C, and 19F) spectroscopy, mass spectrometry, and elemental analysis. The 2-oxazolines were subsequently used as monomers for living cationic ring-opening polymerization (CROP) with microwave irradiation as the heat source (T= 140°C), nitromethane as the solvent, and methyl tosylate as the initiator. The linear first-order kinetic plots of the polymerizations accompanied by a linear increase of the molecular weight with conversion and low polydispersity index (PDI) values (generally below 1.30) indicate a living polymerization mechanism. The resulting polymerization rates reflect a strong sensitivity to the quantity of fluorine substituents in general and the presence or absence of ortho-fluoro substituents of the phenyl ring in particular. All the polymers were isolated and characterized by size-exclusion chromatography and MALDI-TOF mass spectrometry. Finally, a detailed investigation of selected polymer properties was performed by using differential scanning calorimetry, thermogravimetric analysis, and contact-angle measurements, thus resulting in structure-property relationships. Whereas the thermal properties of the polymers are mostly influenced by the presence of ortho-fluoro substituents, the surface properties are mainly determined by the presence of para- and/or metafluoro substituents.

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