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4-[1-Fluoro-meth-(E)-ylidene]-2,3-diphenyl-isoxazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98857-93-3 Structure
  • Basic information

    1. Product Name: 4-[1-Fluoro-meth-(E)-ylidene]-2,3-diphenyl-isoxazolidine
    2. Synonyms: 4-[1-Fluoro-meth-(E)-ylidene]-2,3-diphenyl-isoxazolidine
    3. CAS NO:98857-93-3
    4. Molecular Formula:
    5. Molecular Weight: 255.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98857-93-3.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-[1-Fluoro-meth-(E)-ylidene]-2,3-diphenyl-isoxazolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[1-Fluoro-meth-(E)-ylidene]-2,3-diphenyl-isoxazolidine(98857-93-3)
    11. EPA Substance Registry System: 4-[1-Fluoro-meth-(E)-ylidene]-2,3-diphenyl-isoxazolidine(98857-93-3)
  • 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: 98857-93-3(Hazardous Substances Data)

98857-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98857-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,5 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 98857-93:
(7*9)+(6*8)+(5*8)+(4*5)+(3*7)+(2*9)+(1*3)=213
213 % 10 = 3
So 98857-93-3 is a valid CAS Registry Number.

98857-93-3Downstream Products

98857-93-3Relevant articles and documents

The Cycloadditions of Nitrones with Fluoroallene

Dolbier, William R.,Wicks, Gene E.,Burkholder Conrad R.

, p. 2196 - 2201 (2007/10/02)

Cycloadditions of nitrones with fluoroallene proceed regiospecifically and with a remarkable stereochemical preference for addition syn to the fluorine substituent.The effects of solvent polarity on the rates and stereochemistry of these cycloadditions are reported and discussed.In general these effects are consistent with those reported for other nitrone cycloadditions, and the activation parameters are also similar.

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