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Boronic acid, [4-[difluoro(3,4,5-trifluorophenoxy)methyl]-3,5-difluorophenyl]-, is a complex chemical compound characterized by a boronic acid functional group and fluorinated phenyl rings. It is recognized for its high chemical reactivity and potential biological activity due to the presence of difluoro and trifluorophenoxy groups. Boronic acid,
[4-[difluoro(3,4,5-trifluorophenoxy)methyl]-3,5-difluorophenyl]is widely utilized in organic synthesis and medicinal chemistry as a key building block for the creation of pharmaceuticals and agrochemicals.

685563-69-3

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685563-69-3 Usage

Uses

Used in Organic Synthesis:
Boronic acid, [4-[difluoro(3,4,5-trifluorophenoxy)methyl]-3,5-difluorophenyl]-, is used as a building block in organic synthesis for the production of various pharmaceuticals and agrochemicals. Its unique structure and reactivity allow for the formation of stable complexes with diols, facilitating the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, this boronic acid compound is employed as a precursor for the development of new drugs. Its chemical properties and potential biological activity make it a promising candidate for the design and synthesis of novel therapeutic agents.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
Boronic acid, [4-[difluoro(3,4,5-trifluorophenoxy)methyl]-3,5-difluorophenyl]-, is utilized in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds in organic molecules. This reaction is a powerful tool in organic synthesis, enabling the formation of new chemical entities with potential applications in various industries, including pharmaceuticals and materials science.
Used in Drug Development:
This specific boronic acid compound with difluoro and trifluorophenoxy substituents has potential applications in the development of new drugs. Its unique structure and reactivity can be leveraged to design and synthesize novel therapeutic agents with improved efficacy and selectivity.
Used in Materials Science:
In materials science, Boronic acid, [4-[difluoro(3,4,5-trifluorophenoxy)methyl]-3,5-difluorophenyl]-, can be used to develop new materials with specific properties. Its chemical reactivity and potential to form stable complexes can be harnessed to create materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials for specific industries.

Check Digit Verification of cas no

The CAS Registry Mumber 685563-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,5,6 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 685563-69:
(8*6)+(7*8)+(6*5)+(5*5)+(4*6)+(3*3)+(2*6)+(1*9)=213
213 % 10 = 3
So 685563-69-3 is a valid CAS Registry Number.

685563-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[difluoro-(3,4,5-trifluorophenoxy)methyl]-3,5-difluorobenzene-1-boronic acid

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:685563-69-3 SDS

685563-69-3Relevant academic research and scientific papers

3-pentenyl-terminated difluoroether compounds and synthesis method thereof

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Paragraph 0121-0124, (2021/05/19)

The invention discloses 3-pentenyl-terminated difluoroether compounds and a preparation method thereof. The structure of the compounds is shown as a formula A. According to the compounds provided by the invention, a composition containing the compounds also has a relatively wide nematic phase temperature range, a relatively large Kave value and relatively high transmittance under the condition of maintaining proper optical anisotropy and dielectric anisotropy. The preparation method of the compounds is high in yield, short in reaction time, reasonable in design, simple to operate and suitable for industrial production.

Super-fluorinated liquid crystals: Towards the limits of polarity

Kirsch, Peer,Binder, Werner,Hahn, Alexander,Jaehrling, Kai,Lenges, Marc,Lietzau, Lars,Maillard, David,Meyer, Volker,Poetsch, Eike,Ruhl, Andreas,Unger, Gerald,Froehlich, Roland

scheme or table, p. 3479 - 3487 (2009/04/19)

Highly fluorinated liquid crystals with unprecedented polarity were obtained by introducing a tetrahydropyran moiety into their mesogenic core structure. The new materials exhibit an unusually favourable combination of mesophase properties, excellent solubility and low rotational viscosity, which renders them highly attractive for application in fast-switching active matrix LCDs. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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