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55119-10-3

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55119-10-3 Usage

Description

1,3,6-Tribromo-9H-carbazole is an organic compound belonging to the carbazole family, characterized by the presence of three bromine atoms at the 1, 3, and 6 positions. It is a valuable compound in various fields due to its unique properties and potential applications.

Uses

Used in Environmental and Research Applications:
1,3,6-Tribromo-9H-carbazole is used as a standard in environmental and research applications for its ability to provide accurate and reliable measurements in various analytical techniques.
Used in the Photovoltaic Industry:
1,3,6-Tribromo-9H-carbazole is used as a carbazole-based hole transporting material in the development of cost-effective and environmentally friendly perovskite solar cells. Its incorporation enhances the efficiency and stability of these solar cells, making them more viable for large-scale deployment.
Used in Pharmaceutical Applications:
1,3,6-Tribromo-9H-carbazole serves as an aryl hydrocarbon receptor agonist, which plays a crucial role in the regulation of gene expression and cellular responses. This property makes it a valuable compound for the development of new drugs and therapies.
Used in Chemical Characterization:
1,3,6-Tribromo-9H-carbazole is used for the characterization of monoto tetra-halogenated carbazoles, providing insights into their chemical properties and potential applications. This information is essential for the development of new materials and compounds with tailored properties for various industries.
Used in Biological Potency Studies:
1,3,6-Tribromo-9H-carbazole is utilized in the assessment of the biological potency of monoto tetra-halogenated carbazoles. Understanding the biological effects of these compounds is crucial for their safe and effective use in various applications, including pharmaceuticals and environmental monitoring.

Check Digit Verification of cas no

The CAS Registry Mumber 55119-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55119-10:
(7*5)+(6*5)+(5*1)+(4*1)+(3*9)+(2*1)+(1*0)=103
103 % 10 = 3
So 55119-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H6Br3N/c13-6-1-2-11-8(3-6)9-4-7(14)5-10(15)12(9)16-11/h1-5,16H

55119-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,6-tribromo-9H-carbazole

1.2 Other means of identification

Product number -
Other names HMS547F21

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:55119-10-3 SDS

55119-10-3Upstream product

55119-10-3Relevant articles and documents

A new method for bromination of carbazoles, β-carbolines and iminodibenzyls by use of N-bromosuccinimide and silica gel

Smith, Keith,Martin James,Mistry, Anil G.,Bye, Martin R.,John Faulkner

, p. 7479 - 7488 (2007/10/02)

Carbazole, N-ethylcarbazole, iminodibenzyl (10,11-dihydro-5H-dibenz[b,f]azepine), N-ethyliminodibenzyl and imipramine are readily mono-, di- or polybrominated in high yields at ambient temperature in dichloromethane by use of the appropriate quantity of N-bromosuccinimide in the presence of silica gel. By contrast, the brominations of the β-carbolines, harmane and norharman, are less selective and give mixtures of products, some of which have unusual substitution patterns.

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