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1034306-90-5

6,7-diphenyl-5,12-dihydroindolo[3,2-a]carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1034306-90-5 Structure

  • Basic information

    1. Product Name: 6,7-diphenyl-5,12-dihydroindolo[3,2-a]carbazole
    2. Synonyms: 6,7-diphenyl-5,12-dihydroindolo[3,2-a]carbazole
    3. CAS NO:1034306-90-5
    4. Molecular Formula:
    5. Molecular Weight: 408.502
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1034306-90-5.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: 6,7-diphenyl-5,12-dihydroindolo[3,2-a]carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,7-diphenyl-5,12-dihydroindolo[3,2-a]carbazole(1034306-90-5)
    11. EPA Substance Registry System: 6,7-diphenyl-5,12-dihydroindolo[3,2-a]carbazole(1034306-90-5)

  • 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: 1034306-90-5(Hazardous Substances Data)

1034306-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034306-90-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,3,0 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1034306-90:
(9*1)+(8*0)+(7*3)+(6*4)+(5*3)+(4*0)+(3*6)+(2*9)+(1*0)=105
105 % 10 = 5
So 1034306-90-5 is a valid CAS Registry Number.

1034306-90-5Relevant articles and documents

Modifications of 5,12-dihydroindolo[3,2-a]carbazole scaffold via its regioselective C2,9-formylation and C2,9-acetylation

Kazin, Nikita A.,Demina, Nadezhda S.,Irgashev, Roman A.,Zhilina, Ekaterina F.,Rusinov, Gennady L.

, p. 4686 - 4696 (2019)

The effective approaches for regioselective double formylation and acetylation of 5,12-dialkyl-6,7-diaryl-substituted 5,12-dihydroindolo[3,2-a]carbazoles by their treatment with dichloromethyl methyl ether in the presence of SnCl4 or with acetyl chloride in the presence of AlCl3 to afford the 2,9-diformyl or 2,9-diacetyl derivatives, respectively, were developed. Furthermore, new 2,9-bis(2,2-dicyanovinyl) derivatives were synthesized by the Knoevenagel condensation of diformyl-containing substrates with malononitrile, when new 2,9-bis(quinoxaline-2-yl)- and 2,9-bis(benzo[g]quinoxaline-2-yl) derivatives were formed via microwave-promoted oxidation of diacetyl-containing substrates with SeO2 to the corresponding diglyoxals, followed by the reaction of these intermediates with o-phenylendiamine or 2,3-diaminonaphthalene, respectively. The basic optical and electrochemical properties of some 5,12-dihydroindolo[3,2-a]carbazoles were investigated.

Condensation of Indoline with Some 1,2- and 1,3-Diketones

Kilic, Haydar,Aydin, Omer,Bayindir, Sinan,Saracoglu, Nurullah

, p. 2096 - 2101 (2016/11/23)

Bismuth nitrate catalyzed condensation reactions of indoline with 1,2- and 1,3-diketones were investigated and were reported to proceed via different reaction pathways with the involvement of one or two of the carbonyl groups. While the reaction of indoli

Charge-transporting varnish, charge-transporting thin film and method for manufacturing same, and organic electroluminescent element and method for manufacturing same

-

Paragraph 0088-0089, (2017/04/03)

The present invention includes: a charge-transporting substance composed of an indolocarbazole represented by formula (1), a dopant, and an organic solvent.

An efficient synthesis of indolo[3,2-a]carbazoles via the novel acid catalyzed reaction of indoles and diaryl-1,2-diones

Nair, Vijay,Nandialath, Vidya,Abhilash, Keecherikunnel G.,Suresh, Eringathodi

experimental part, p. 1738 - 1742 (2008/10/09)

A mild and efficient one pot method for the synthesis of indolo[3,2-a]carbazole derivatives by the para-toluenesulfonic acid catalyzed condensation of indole with acyclic 1,2-diones is described. With cyclobutene-1,2-diones the reaction afforded indole substituted carbazole derivatives in good yield. The Royal Society of Chemistry.

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