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13438-50-1

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13438-50-1 Usage

Description

3-Bromofluoranthene is an organic compound that serves as a key intermediate in the synthesis of various chemical compounds, particularly in the production of 3-Methylfluoranthene, an environmental pollutant known for its tumor-initiating properties.

Uses

Used in Chemical Synthesis:
3-Bromofluoranthene is used as an intermediate in the synthesis of 3-Methylfluoranthene (M305315), an environmental pollutant that acts as an active tumor initiator. This synthesis process is crucial for understanding the formation and impact of such pollutants on human health and the environment.
Used in Environmental Research:
3-Bromofluoranthene plays a significant role in environmental research, particularly in studying the effects of 3-Methylfluoranthene on ecosystems and human health. By understanding the synthesis and properties of 3-Bromofluoranthene, researchers can better evaluate the risks associated with exposure to 3-Methylfluoranthene and develop strategies for mitigating its impact.
Used in Pharmaceutical Development:
Although not explicitly mentioned in the provided materials, 3-Bromofluoranthene may also have potential applications in the development of pharmaceuticals, given its role as a synthetic intermediate. Its unique chemical structure could be utilized in the creation of new drugs or drug delivery systems, contributing to advancements in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 13438-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13438-50:
(7*1)+(6*3)+(5*4)+(4*3)+(3*8)+(2*5)+(1*0)=91
91 % 10 = 1
So 13438-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H9Br/c17-15-9-8-13-11-5-2-1-4-10(11)12-6-3-7-14(15)16(12)13/h1-9H

13438-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromofluoranthene

1.2 Other means of identification

Product number -
Other names 3-bromofluoranthene

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:13438-50-1 SDS

13438-50-1Relevant articles and documents

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Altschuler,L.,Berliner,E.

, p. 5837 - 5845 (1966)

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Phosphoryl substituted Fluoranthene derivatives and organic electroluminescent device including the same

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Paragraph 0089-0091, (2016/11/28)

Provided are phosphoryl group bonded fluoranthene derivatives represented by chemical formula 1. In chemical formula 1, the definition of each substituent group is the same as described in the specification. The fluoranthene derivatives have excellent current density and durability in comparison to a conventional material, and can be used to an organic electroluminescent device, thereby lowering the driving voltage and improving luminous efficiency while extending the lifespan.

NOVEL COMPOUNDS FOR ORGANIC ELECTRONIC MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME

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Page/Page column 15-16, (2012/03/26)

Provided are novel compounds for organic electronic material and an organic electroluminescent device using the same. Because the compounds for organic electronic material according to the present invention are highly efficient at transporting electrons, crystallization is prevented when manufacturing a device and current properties of the device are improved due to favorably formed layers. Accordingly, OLED devices having improved power efficiency as well as reduced operating voltage can be manufactured.

Synthesis of fluoranthenes by hydroarylation of alkynes catalyzed by gold(I) or gallium trichloride

Pascual, Sergio,Bour, Christophe,Mendoza, Paula De,Echavarren, Antonio M.

, p. 1520 - 1525 (2012/02/04)

Electrophilic gold(I) catalyst 6 competes with GaCl3 as the catalyst of choice in the synthesis of fluoranthenes by intramolecular hydroarylation of alkynes. The potential of this catalyst for the preparation of polyarenes is illustrated by a s

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