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2-Bromo-4-fluoro-1-((3-fluorobenzyl)oxy)benzene is a chemical compound characterized by its molecular formula C13H8BrF2O and a molecular weight of 305.1 g/mol. It is a benzene derivative that incorporates bromine, fluorine, and oxygen atoms within its structure. 2-Bromo-4-fluoro-1-((3-fluorobenzyl)oxy)benzene is recognized for its potential in various organic synthesis reactions and pharmaceutical research, with the capacity to contribute to the development of new drugs and materials. The presence of halogen atoms in its structure endows it with unique reactivity and properties, positioning it as a valuable entity in the realms of medicinal chemistry and material science.

1019446-41-3

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1019446-41-3 Usage

Uses

Used in Organic Synthesis:
2-Bromo-4-fluoro-1-((3-fluorobenzyl)oxy)benzene is used as a key intermediate in organic synthesis for the creation of complex organic molecules. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Bromo-4-fluoro-1-((3-fluorobenzyl)oxy)benzene is utilized as a starting material or a building block in the development of new drugs. Its structural features make it a promising candidate for the design of novel therapeutic agents.
Used in Medicinal Chemistry:
2-Bromo-4-fluoro-1-((3-fluorobenzyl)oxy)benzene is employed as a component in medicinal chemistry for the exploration of its potential biological activities. The presence of halogens may impart specific properties that are advantageous for drug-target interactions.
Used in Material Science:
In the field of material science, 2-Bromo-4-fluoro-1-((3-fluorobenzyl)oxy)benzene is used for the development of new materials with unique properties. Its halogenated structure may contribute to the creation of materials with enhanced performance characteristics.
Overall, 2-Bromo-4-fluoro-1-((3-fluorobenzyl)oxy)benzene is a significant chemical with a broad spectrum of applications across scientific and industrial domains, underscoring its importance in modern chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1019446-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,9,4,4 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1019446-41:
(9*1)+(8*0)+(7*1)+(6*9)+(5*4)+(4*4)+(3*6)+(2*4)+(1*1)=133
133 % 10 = 3
So 1019446-41-3 is a valid CAS Registry Number.

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