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114468-92-7

4-phenyl-2,3-phenantrenedicarboxylic acid anhydride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114468-92-7 Structure

  • Basic information

    1. Product Name: 4-phenyl-2,3-phenantrenedicarboxylic acid anhydride
    2. Synonyms: 4-phenyl-2,3-phenantrenedicarboxylic acid anhydride
    3. CAS NO:114468-92-7
    4. Molecular Formula:
    5. Molecular Weight: 324.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114468-92-7.mol
    9. Article Data: 2

  • 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-phenyl-2,3-phenantrenedicarboxylic acid anhydride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-phenyl-2,3-phenantrenedicarboxylic acid anhydride(114468-92-7)
    11. EPA Substance Registry System: 4-phenyl-2,3-phenantrenedicarboxylic acid anhydride(114468-92-7)

  • 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: 114468-92-7(Hazardous Substances Data)

114468-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114468-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,6 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114468-92:
(8*1)+(7*1)+(6*4)+(5*4)+(4*6)+(3*8)+(2*9)+(1*2)=127
127 % 10 = 7
So 114468-92-7 is a valid CAS Registry Number.

114468-92-7Relevant articles and documents

Phthalocyanines and related compounds: XXXIX. Synthesis of derivatives of some substituted 1-phenylnaphthalene-2,3-dicarboxylic acids

Donyagina,Luk''yanets

, p. 795 - 799 (2007/10/03)

Derivatives (dinitriles, anhydrides, imides, N-phenylimides) of substituted 1-phenylnaphthalene-2,3-dicarboxylic and 1-phenylphenanthrene-2,3-dicarboxylic acids were prepared by the reactions of 2-bromomethylbenzophenones with various dienophiles. Starting from these derivatives, gallium complexes of substituted tetra-1-phenyl-2,3-naphthalocyanines and tetra(1-phenyl-2,3-phenanthro) porphyrazine were synthesized. 2005 Pleiades Publishing, Inc.

1-Phenylisobenzofuran, 1-Phenylnaphthofuran, 1-Phenylnaphthofuran, and 3-Phenylnaphthofuran via Cyclic Hemiaminal, Hemiacetal, and Acetal Precursors

Smith, James G.,Fogg, Deryn E.,Munday, Ian J.,Sandborn, Richard E.,Dibble, Peter W.

, p. 2942 - 2953 (2007/10/02)

The title compounds have been generated via cyclic hemiaminal, hemiacetal, and acetal precursors and trapped in Diels-Alder reactions with several dienophiles.The precursors are easily prepared from o-bromobenzyl alcohol, 2-bromo-3-naphthalenemethanol, or

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