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CAS

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123542-16-5

10-ethyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-4,9-epiminobenzo[f]isoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123542-16-5 Structure

  • Basic information

    1. Product Name: 10-ethyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-4,9-epiminobenzo[f]isoindole-1,3(2H)-dione
    2. Synonyms: 10-ethyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-4,9-epiminobenzo[f]isoindole-1,3(2H)-dione
    3. CAS NO:123542-16-5
    4. Molecular Formula:
    5. Molecular Weight: 318.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123542-16-5.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: 10-ethyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-4,9-epiminobenzo[f]isoindole-1,3(2H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 10-ethyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-4,9-epiminobenzo[f]isoindole-1,3(2H)-dione(123542-16-5)
    11. EPA Substance Registry System: 10-ethyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-4,9-epiminobenzo[f]isoindole-1,3(2H)-dione(123542-16-5)

  • 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: 123542-16-5(Hazardous Substances Data)

123542-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123542-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,5,4 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123542-16:
(8*1)+(7*2)+(6*3)+(5*5)+(4*4)+(3*2)+(2*1)+(1*6)=95
95 % 10 = 5
So 123542-16-5 is a valid CAS Registry Number.

123542-16-5Downstream Products

123542-16-5Relevant articles and documents

Reduction of Benzolactams to Isoindoles via an Alkoxide-Catalyzed Hydrosilylation

Ding, Guangni,Wu, Xiaoyu,Jiang, Lili,Zhang, Zhaoguo,Xie, Xiaomin

, p. 6048 - 6051 (2017)

An alkoxide-catalyzed reduction of benzolactams to isoindoles with silanes was realized. With t-BuOK as the catalyst and Ph2SiH2 as the reductant, a series of benzolactams containing different functional groups were reduced to the co

Studies on the Chemistry of Isoindoles and Isoindolenines, XXXVI. - Reactions of 2-Alkyl-2H-isoindoles with Maleic Imides

Kreher, Richard P.,Seubert, Juergen,Schmitt, Dieter,Use, Goetz,Kohl, Norbert,Muleta, Tilahun

, p. 381 - 390 (2007/10/02)

2-Alkyl-2H-isoindoles 2 react with maleic imides 4 exclusively in position 1 and 3 by cycloaddition to form Diels-Alder adducts.The transformation of the endo isomers 6 into the thermodynamically more stable exo isomers 7 depends on the dienophile.The cyc

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