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Carbazol-9-yl-pyridin-3-yl-methanone is a complex organic compound with the molecular formula C21H14N2O. It is characterized by a carbazolyl group (a derivative of carbazole) attached to a pyridinyl group (a derivative of pyridine) through a methanone (ketone) linker. This molecule is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or materials science due to its unique structure and properties. The compound's specific chemical behavior and reactivity are determined by the interaction of its constituent functional groups, which can influence its stability, solubility, and potential interactions with other molecules.

7469-85-4

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7469-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7469-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7469-85:
(6*7)+(5*4)+(4*6)+(3*9)+(2*8)+(1*5)=134
134 % 10 = 4
So 7469-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H12N2O/c21-18(13-6-5-11-19-12-13)20-16-9-3-1-7-14(16)15-8-2-4-10-17(15)20/h1-12H

7469-85-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name carbazol-9-yl(pyridin-3-yl)methanone

1.2 Other means of identification

Product number -
Other names Methanone,9H-carbazol-9-yl-3-pyridinyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7469-85-4 SDS

7469-85-4Downstream Products

7469-85-4Relevant academic research and scientific papers

A versatile route to benzocanthinones

Markgraf, J. Hodge,Dowst, Adrian A.,Hensley, Laurel A.,Jakobsche, Charles E.,Kaltner, Cindy J.,Webb, Peter J.,Zimmerman, Patrick W.

, p. 9102 - 9110 (2005)

Benzocanthinone (1) and five analogs (10, 12-15) were prepared by radical-induced cyclizations of halo N-aroyl derivatives of β-carboline and carbazole.

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