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Isoindolo[2,1-a]indol-6-one is a complex organic compound with the molecular formula C16H7NO. It is a tricyclic structure, consisting of two fused indole rings and an isoindole ring. isoindolo[2,1-a]indol-6-one is known for its unique electronic properties and potential applications in the field of materials science, particularly in the development of organic semiconductors and optoelectronic devices. The structure of isoindolo[2,1-a]indol-6-one features a central nitrogen atom that contributes to its electronic properties, making it an interesting candidate for further research and development in the realm of advanced materials.

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  • 4992-09-0 Structure
  • Basic information

    1. Product Name: isoindolo[2,1-a]indol-6-one
    2. Synonyms: isoindolo[2,1-a]indol-6-one
    3. CAS NO:4992-09-0
    4. Molecular Formula:
    5. Molecular Weight: 219.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4992-09-0.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: isoindolo[2,1-a]indol-6-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: isoindolo[2,1-a]indol-6-one(4992-09-0)
    11. EPA Substance Registry System: isoindolo[2,1-a]indol-6-one(4992-09-0)
  • 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: 4992-09-0(Hazardous Substances Data)

4992-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4992-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4992-09:
(6*4)+(5*9)+(4*9)+(3*2)+(2*0)+(1*9)=120
120 % 10 = 0
So 4992-09-0 is a valid CAS Registry Number.

4992-09-0Relevant articles and documents

Pd-Catalyzed Cyclocarbonylation of 2-(2-Bromoaryl)indoles with CO as a C1 Source: Selective Access to 6 H-Isoindolo[2,1-a]indol-6-ones and Indeno[1,2-b]indol-10(5 H)-ones

Guo, Shenghai,Tao, Li,Wang, Fang,Fan, Xuesen

, p. 3090 - 3096 (2016/11/13)

A highly efficient and regioselective synthetic route to 6 H-isoindolo[2,1-a]indol-6-ones and indeno[1,2-b]indol-10(5 H)-ones through the Pd-catalyzed cyclocarbonylation of 2-(2-bromoaryl)indoles under atmospheric CO pressure has been achieved. Notably, the regioselectivity of the reaction was exclusively dependent on the structural characteristics of the indole substrates. With N-unsubstituted indoles as the starting materials, the reaction afforded 6H-isoindolo[2,1-a]indol-6-ones in good-to-excellent yields. On the other hand, with N-substituted indoles as the substrates, the reaction gave indeno[1,2-b]indol-10(5 H)-ones in a highly regioselective manner.

OXIDATION OF 1-BENZOYLPYRROLE AND 1-AROYLINDOLES BY PALLADIUM ACETATE

Itahara, Toshio

, p. 2557 - 2562 (2007/10/02)

Oxidation of 1-benzoylpyrrole and 1-aroylindoles by palladium acetate in acetic acid gave the corresponding ring-closed products and dimerized compounds.

Alkenylation of 1-Acylindoles with Olefins Bearing Electron-withdrawing Substituents and Palladium Acetate

Itahara, Toshio,Ikeda, Mizue,Sakakibara, Tsutomu

, p. 1361 - 1363 (2007/10/02)

The oxidation of 1-(2,6-dichlorobenzoyl)indole with olefins, such as alkyl acrylates and acrylonitrile, and palladium acetate resulted in selective 3-alkenylation of the indole nucleus.Treatment of 1-acyl-3-methylindoles under similar conditions gave the corresponding 2-alkenyl substituted indoles, while the oxidation of 6-oxo-6H-isoindoloindole gave the corresponding 3-alkenyl substituted indoles.

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