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341-41-3

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341-41-3 Usage

Description

1-Bromo-4-fluoronaphthalene is a solid, polycyclic aromatic compound characterized by the presence of a bromine and a fluorine atom in its molecular structure. It is a significant intermediate in the synthesis of various complex organic molecules and materials.

Uses

1. Used in Materials Science:
1-Bromo-4-fluoronaphthalene is used as a starting material for the synthesis of Fluorobenzo[c]fluoren (F588435), a polycyclic aromatic hydrocarbon with extensive applications in the field of materials science. Its unique structure and properties make it a valuable component in the development of advanced materials for organic electronics, light-emitting diodes (LEDs), and solar cells.
2. Used in Organic Electronics:
In the organic electronics industry, 1-Bromo-4-fluoronaphthalene serves as a crucial precursor for the synthesis of compounds that exhibit excellent electronic properties. These synthesized materials find applications in the development of high-performance electronic devices, such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs).
3. Used in Light Emitting Diodes (LEDs):
1-Bromo-4-fluoronaphthalene is used as a key intermediate in the production of advanced materials for light-emitting diodes. The synthesized compounds based on this intermediate exhibit improved luminescent properties, leading to more efficient and longer-lasting LEDs.
4. Used in Solar Cells:
In the solar cell industry, 1-Bromo-4-fluoronaphthalene is utilized as a starting material for the synthesis of novel materials with enhanced photovoltaic properties. These materials contribute to the development of more efficient and cost-effective solar cells, paving the way for sustainable energy solutions.
5. Used in Chemical Research:
1-Bromo-4-fluoronaphthalene is also employed as a valuable compound in chemical research, particularly in the study of polycyclic aromatic hydrocarbons and their derivatives. Its unique structure and properties make it an interesting subject for exploring new synthetic routes, reaction mechanisms, and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 341-41-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 341-41:
(5*3)+(4*4)+(3*1)+(2*4)+(1*1)=43
43 % 10 = 3
So 341-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H6BrF/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H

341-41-3 Well-known Company Product Price

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  • Alfa Aesar

  • (A16934)  1-Bromo-4-fluoronaphthalene, 98%   

  • 341-41-3

  • 1g

  • 516.0CNY

  • Detail
  • Alfa Aesar

  • (A16934)  1-Bromo-4-fluoronaphthalene, 98%   

  • 341-41-3

  • 5g

  • 1730.0CNY

  • Detail
  • Alfa Aesar

  • (A16934)  1-Bromo-4-fluoronaphthalene, 98%   

  • 341-41-3

  • 25g

  • 7180.0CNY

  • Detail

341-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-4-FLUORONAPHTHALENE

1.2 Other means of identification

Product number -
Other names 1-fluoro-4-bromonaphthalene

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:341-41-3 SDS

341-41-3Relevant articles and documents

4-fluoronaphthalene-1-alcohol preparation technology

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Paragraph 0009; 0020; 0021; 0029; 0030; 0038; 0039; 0047, (2017/08/26)

The invention discloses a 4-fluoronaphthalene-1-alcohol preparation technology. The preparation technology takes 1-fluoronaphthalene as a raw material, the raw material is subjected to halogenation, boration and hydrolysis to obtain the 4-fluoronaphthalene-1-alcohol, and the overall yield can reach 60%. The technology has the advantages of low cost and easy acquisition of the raw materials, simple and easy operation of post-treatment t, high yield, and easy industrial application.

2-aminopyridines containing fused ring substituents

-

, (2008/06/13)

The present invention relates to 2-aminopyridine derivatives of the formula wherein G, R1 and R2 are defined as in the specification, that exhibit activity as nitric oxide synthase (NOS) inhibitors, to pharmaceutical compositions containing them and to their use in the treatment and prevention of central nervous system and other disorders.

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