63077-00-9

Basic information

• Product Name: 12,13-Dihydro-7H-dibenzo[a,g]carbazole
• Synonyms: 12,13-Dihydro-7H-dibenzo[a,g]carbazole
• CAS NO: 63077-00-9
• Molecular Formula: C₂₀H₁₅N
• Molecular Weight: 269.36
• Mol File: 63077-00-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 402.48°C (rough estimate)
• Flash Point: 231.1°C
• Appearance: /
• Density: 0.9788 (rough estimate)
• Vapor Pressure: 3.71E-10mmHg at 25°C
• Refractive Index: 1.7800 (estimate)
• CAS DataBase Reference: 12,13-Dihydro-7H-dibenzo[a,g]carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 12,13-Dihydro-7H-dibenzo[a,g]carbazole(63077-00-9)
• EPA Substance Registry System: 12,13-Dihydro-7H-dibenzo[a,g]carbazole(63077-00-9)

Safety Data

• Hazardous Substances Data: 63077-00-9(Hazardous Substances Data)

Usage

Appearance

Yellowish-brown powder

Solubility

Insoluble in water

Chemical classification

Polycyclic aromatic hydrocarbon compound

Primary use

Building block in the synthesis of organic electronic materials

Examples

Semiconducting polymers, organic light emitting diodes (OLEDs)

Potential application

Photosensitizer in photodynamic therapy

Explanation

Treatment that uses light-activated compounds to kill cancer cells

Environmental impact

Known environmental contaminant

Health effects

Potential carcinogen

Ongoing research

Investigating properties and potential applications
These properties and contents provide a comprehensive overview of 12,13-Dihydro-7H-dibenzo[a,g]carbazole, highlighting its chemical structure, appearance, solubility, and various applications in the field of organic electronics and medicine. Additionally, it emphasizes the importance of understanding its environmental and health effects due to its status as a contaminant and potential carcinogen.

InChI:InChI=1/C20H15N/c1-3-7-15-13(5-1)10-12-18-19(15)17-11-9-14-6-2-4-8-16(14)20(17)21-18/h1-8,10,12,21H,9,11H2

Upstream product

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Downstream Products

• 207-84-1 7H-dibenzo[a,g]carbazole 

Relevant articles and documents

Development of a Unique Class of Spiro-Type Two-Photon Functional Fluorescent Dyes and Their Applications for Sensing and Bioimaging

Spiro compounds with rigid structures have attracted significant attention in the recent years due to their useful applications in diverse fields such as asymmetric catalysis and organic optoelectronic materials. However, spiro cores have not yet been employed as the spiro-type two-photon fluorescent dyes in the aspects of sensing and bioimaging. Therefore, the spiro-type two-photon fluorescent dyes with excellent two-photon properties are highly sought after. Here, a unique class of spiro-type two-photon fluorescent dyes (STP) is engineered and applied in sensing and bioimaging. The studies indicate that the novel STP fluorescent dyes have favorable two-photon properties from the point view of spiro compounds. By exploiting the superior two-photon optical properties of the STP dyes, the first two-photon ratiometric HOCl fluorescent probe STP-HClO for sensing and imaging HOCl in the living cells and living tissues is constructed, demonstrating the profound value of the new STP dyes for the unprecedented development of the sprio-type fluorescent sensing and imaging agents. It is believed that the innovative STP dyes may pave the way for designing more efficient spiro-type two-photon fluorescent probes and organic optoelectronic materials as well.

Syntheses of 2-substituted indoles and fused indoles by photostimulated reactions of o-iodoanilines with carbanions by the SRN1 mechanism

2-Substituted indoles (5a,b and 7) and fused indoles (9a-c, 11a,b, and 12) have been obtained by the SRN1 mechanism from photostimulated reactions of o-iodoaniline (1) and 1-halo-2-naphthalen-2-ylamines (3a,b) with enolate ions of acyclic (acet