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1,3-Dibromo-2-fluorobenzene is an organobromine compound, specifically an aromatic halide, which consists of a benzene ring substituted with two bromine atoms and one fluorine atom. The bromine atoms are positioned in the 1 and 3 spots on the benzene ring, while the fluorine atom is in the 2 spot. It is less common than other aromatic halides but is occasionally used in the synthesis of other compounds. Based on its molecular weight and structure, it is expected to be a mid to high boiling liquid under standard conditions. 1,3-dibroMo-2-fluorobenzene is typically produced and handled under controlled conditions due to the reactivity of the bromine and fluorine atoms.

1435-54-7

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1435-54-7 Usage

Uses

Used in Chemical Synthesis:
1,3-Dibromo-2-fluorobenzene is used as an intermediate in the synthesis of various organic compounds. Its unique structure with two bromine atoms and one fluorine atom allows for selective reactions and functional group transformations, making it a valuable building block in the preparation of complex molecules.
Used in Pharmaceutical Industry:
1,3-Dibromo-2-fluorobenzene is used as a starting material for the development of new pharmaceutical compounds. Its reactivity and structural features enable the creation of novel drug candidates with potential therapeutic applications.
Used in Material Science:
1,3-Dibromo-2-fluorobenzene is used as a precursor in the synthesis of advanced materials, such as polymers and coatings, that exhibit unique properties due to the presence of bromine and fluorine atoms. These materials can be tailored for specific applications, such as flame retardancy or enhanced chemical stability.
Used in Research and Development:
1,3-Dibromo-2-fluorobenzene is used as a research compound in academic and industrial laboratories. Its reactivity and structural characteristics make it an interesting subject for studying reaction mechanisms, exploring new synthetic routes, and understanding the effects of halogen substitution on molecular properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1435-54-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1435-54:
(6*1)+(5*4)+(4*3)+(3*5)+(2*5)+(1*4)=67
67 % 10 = 7
So 1435-54-7 is a valid CAS Registry Number.

1435-54-7SDS

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 1,3-Dibromo-2-fluorobenzene

1.2 Other means of identification

Product number -
Other names 1,3-dibromo-2-fluorobenzene

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:1435-54-7 SDS

1435-54-7Upstream product

1435-54-7Relevant academic research and scientific papers

BORON-CONTAINING SMALL MOLECULES

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Paragraph 0352; 0353, (2013/06/04)

This invention provides novel compounds, methods of using the compounds, and pharmaceutical formulations comprising the compounds.

Preparation process of fluorine substituted aromatic compound

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, (2008/06/13)

A preparation process of a fluorine substituted aromatic compound comprising reacting an alkali metal or alkali earth metal salt of an aromatic compound having a hydroxy group with an organic fluorinating agent is disclosed. As a representative fluorinating agent, a bis-dialkylamino-difluoromethane compound, for example, 2,2′-difluoro-1,3-dimethylimidazolidine, is exemplified. According to the process, an industrially useful fluorinated aromatic compound, for example, a fluorobenzene, a fluorine substituted benzophenone, a fluorine substituted diarylsulfone can be prepared with ease in economy without specific equipment.

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