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2-methyl-6-pentafluorophenoxy-4,5,7-trifluorobenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81794-33-4

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  • 81794-33-4 Structure
  • Basic information

    1. Product Name: 2-methyl-6-pentafluorophenoxy-4,5,7-trifluorobenzofuran
    2. Synonyms: 2-methyl-6-pentafluorophenoxy-4,5,7-trifluorobenzofuran
    3. CAS NO:81794-33-4
    4. Molecular Formula:
    5. Molecular Weight: 368.183
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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-methyl-6-pentafluorophenoxy-4,5,7-trifluorobenzofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl-6-pentafluorophenoxy-4,5,7-trifluorobenzofuran(81794-33-4)
    11. EPA Substance Registry System: 2-methyl-6-pentafluorophenoxy-4,5,7-trifluorobenzofuran(81794-33-4)
  • 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: 81794-33-4(Hazardous Substances Data)

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81794-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81794-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,9 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81794-33:
(7*8)+(6*1)+(5*7)+(4*9)+(3*4)+(2*3)+(1*3)=154
154 % 10 = 4
So 81794-33-4 is a valid CAS Registry Number.

81794-33-4Downstream Products

81794-33-4Relevant academic research and scientific papers

Partially Fluorinated Heterocyclic Compounds. Part 16. Preparation of Furan Derivatives from Pentafluorophenyl and Heptafluoro-2-naphthyl Prop-2-ynyl Ethers with Aromatic Compounds, and the Isolation of Hydrogen-abstraction Products

Brooke, Gerald M.

, p. 107 - 110 (2007/10/02)

Pentafluorophenyl and heptafluoro-2-naphthyl prop-2-ynyl ethers react in N,N-diethylaniline to give among other products 2-methylfuran derivatives formed by hydrogen-abstraction reactions, and 2-(diethylaminobenzyl)furan derivatives ; the 2-fluoromethylfuran (16) is also formed from (5).No aromatic substitution products are obtained from (5) with nitrobenzene or benzylidyne trifluoride.It was not possible to distinguish between homolytic and heterolytic fission of the aliphatic C-F bonds in the Claisen rearrangement intermediates (8) and (9) involved in these reactions.

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