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98453-02-2

11b-phenoxy-5a,6,11-triphenyl-5a,11b-dihydro-naphto<2,3-3',4'>cyclobuta<1',2',-2,3>benzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98453-02-2

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  • 98453-02-2 Structure

  • Basic information

    1. Product Name: 11b-phenoxy-5a,6,11-triphenyl-5a,11b-dihydro-naphto<2,3-3',4'>cyclobuta<1',2',-2,3>benzofuran
    2. Synonyms:
    3. CAS NO:98453-02-2
    4. Molecular Formula:
    5. Molecular Weight: 564.683
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98453-02-2.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: 11b-phenoxy-5a,6,11-triphenyl-5a,11b-dihydro-naphto<2,3-3',4'>cyclobuta<1',2',-2,3>benzofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 11b-phenoxy-5a,6,11-triphenyl-5a,11b-dihydro-naphto<2,3-3',4'>cyclobuta<1',2',-2,3>benzofuran(98453-02-2)
    11. EPA Substance Registry System: 11b-phenoxy-5a,6,11-triphenyl-5a,11b-dihydro-naphto<2,3-3',4'>cyclobuta<1',2',-2,3>benzofuran(98453-02-2)

  • 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: 98453-02-2(Hazardous Substances Data)

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98453-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98453-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98453-02:
(7*9)+(6*8)+(5*4)+(4*5)+(3*3)+(2*0)+(1*2)=162
162 % 10 = 2
So 98453-02-2 is a valid CAS Registry Number.

98453-02-2Relevant articles and documents

Transformations photochimiques d'endoperoxydes derives d'hydrocarbures aromatiques polycycliques V. Cas de I'endoperoxyde de rubrene: formation d'un nouveau type de photo-isomere

Rigaudy, Jean,Cuong, Nguyen Kim,Godard, Jean-Yves

, p. 78 - 83 (2007/10/02)

Photolysis in benzene at long wavelengths (λ>=420 nm) of rubrene endoperoxide. 11 affords mainly the bicyclic acetal 18, accompanied by the rubrene "iso-oxyde" 22 and by a new isomer: 11b-phenoxy-5a,6,11-triphenyl-5a,11b-dihydro-naphto cyclobutabenzo(b)furan 23, the structure of which has been established by 13C NMR.These various compounds result very likely from subsequent isomerizations of the two unstable meso-diepoxydes 13 and 14 arising first in the process.Moreover, diepoxide 14, precursor of 22 and 23, has been trapped by N-methylmaleimide as adduct 15.

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