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2-chloro-9H-pyrido[2,3-b]indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26869-12-5

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26869-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26869-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26869-12:
(7*2)+(6*6)+(5*8)+(4*6)+(3*9)+(2*1)+(1*2)=145
145 % 10 = 5
So 26869-12-5 is a valid CAS Registry Number.

26869-12-5Relevant academic research and scientific papers

TRICYCLIC CRBN LIGANDS AND USES THEREOF

-

, (2020/01/24)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of CRBN, and the treatment of CRBN-mediated disorders.

Organic electroluminescent material and device thereof

-

, (2020/05/14)

Disclosed are an organic electroluminescent material and a device thereof. The organic electroluminescent material adopts a series of new indolocarbazole compounds, and can be used as a main body material, a charge transport material and the like of an el

Organometallic Complex, Light-Emitting Element, Light-Emitting Device, Electronic Device, and Lighting Device

-

, (2017/03/21)

A novel organometallic complex having high reliability is provided. The organometallic complex includes platinum and a ligand coordinated to the platinum. The ligand includes a plurality of pyridoindole skeletons. Each of the pyridoindole skeletons includ

A short entry into the pyrido[2,3-b] indole ring system. Synthesis of the tetracyclic segment of the marine antitumor agents: Grossularines-1 and -2

Achab, Said,Guyot, Michele,Potier, Pierre

, p. 2127 - 2130 (2007/10/02)

A new method for the synthesis of substituted pyrido[2,3-b] indoles (α-carbolines) (14, 27-31), featuring Pd-catalyzed cross coupling between pyridine and aniline derivatives and subsequent intramolecular cylization, has been developed. This method provid

Titanium(0) Reagents; 2. A Selective and Efficient Deoxygenation of Halogen Containing Heteroaromatic N-Oxides

Malinowski, Marek,Kaczmarek, Lukasz

, p. 1013 - 1015 (2007/10/02)

Following successful reductions of unfunctionalized heteroaromatic N-oxides by titanium(0), we applied this method to halogenated aromatic N-oxides to give the deoxygenated halogeno derivatives in 90-95percent yield.

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