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perfluoro-4-methyl-3,4-dihydroisocoumarin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146366-26-9 Structure
  • Basic information

    1. Product Name: perfluoro-4-methyl-3,4-dihydroisocoumarin
    2. Synonyms:
    3. CAS NO:146366-26-9
    4. Molecular Formula:
    5. Molecular Weight: 342.093
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146366-26-9.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: perfluoro-4-methyl-3,4-dihydroisocoumarin(CAS DataBase Reference)
    10. NIST Chemistry Reference: perfluoro-4-methyl-3,4-dihydroisocoumarin(146366-26-9)
    11. EPA Substance Registry System: perfluoro-4-methyl-3,4-dihydroisocoumarin(146366-26-9)
  • 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: 146366-26-9(Hazardous Substances Data)

146366-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146366-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,6 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 146366-26:
(8*1)+(7*4)+(6*6)+(5*3)+(4*6)+(3*6)+(2*2)+(1*6)=139
139 % 10 = 9
So 146366-26-9 is a valid CAS Registry Number.

146366-26-9Downstream Products

146366-26-9Relevant articles and documents

FLUOROINDENES. 13. TRANSFORMATIONS OF POLYFLUORINATED INDENES AND 1-ALKYLIDENEINDANS IN THE H2O2-HF-SbF5 SYSTEM

Chuikov, I. P.,Karpov, V. M.,Platonov, V. E.

, p. 1104 - 1110 (2007/10/02)

The reaction of perfluorinated indene, 3-methylindene, and 1-methylene- and 1-ethylideneindans with hydrogen peroxide in the hydrogen fluoride-antimony pentafluoride medium takes place at the multilple bond of the substrate and leads to the oxo derivatives of indan.The process probably takes place through the electrophilic addition of HO+.The C=C bond in perfluoro-3-methylindenone is not affected.In this compound and also in perfluoro-2-indanone and perfluoro-1-methyl-2-indanone the carbonyl group is involved in reaction with hydrogen peroxide in the HF-SbF5 system, and six-membered oxygen-containing heterocyclic compounds are formed.Keywords: Polyfluorinated indenes, alkylindeneindans, electrophilic hydroxyfluorination, polyfluorinated ketones, Bayer-Villiger reaction.

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