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6-ethoxy-5-(trifluoroMethyl)pyridin-3-ylboronic acid is a boronic acid derivative with the chemical formula C10H12BF3NO3. It is a versatile reagent in organic synthesis and medicinal chemistry, characterized by the presence of both the boronic acid and pyridine functional groups. 6-ethoxy-5-(trifluoroMethyl)pyridin-3-ylboronic acid is highly reactive and is often utilized in the creation of pharmaceutical compounds due to its ability to form carbon-carbon bonds and target specific biological pathways. The trifluoromethyl substituent further enhances its chemical and biological properties.

849934-85-6

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849934-85-6 Usage

Uses

Used in Organic Synthesis:
6-ethoxy-5-(trifluoroMethyl)pyridin-3-ylboronic acid is used as a building block in organic synthesis for the creation of various pharmaceutical compounds. Its unique structure allows for the formation of carbon-carbon bonds, making it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-ethoxy-5-(trifluoroMethyl)pyridin-3-ylboronic acid is used as a key intermediate in the development of novel drug candidates. Its potential to target specific biological pathways and the unique properties imparted by the trifluoromethyl substituent make it a promising candidate for the design of new therapeutic agents.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
6-ethoxy-5-(trifluoroMethyl)pyridin-3-ylboronic acid is employed as a highly reactive reagent in Suzuki-Miyaura cross-coupling reactions. This palladium-catalyzed reaction allows for the formation of carbon-carbon bonds between the boronic acid derivative and an organic halide or triflate, facilitating the synthesis of a wide range of organic compounds.
Used in Pharmaceutical Industry:
6-ethoxy-5-(trifluoroMethyl)pyridin-3-ylboronic acid is used as a key component in the development of new pharmaceuticals. Its versatility and reactivity make it an essential building block for the synthesis of various drug candidates, particularly those targeting specific biological pathways. The incorporation of the trifluoromethyl group can also enhance the drug's potency and selectivity, leading to more effective treatments.
Used in Chemical Research:
In the realm of chemical research, 6-ethoxy-5-(trifluoroMethyl)pyridin-3-ylboronic acid is utilized as a valuable tool for studying the properties and reactivity of boronic acid derivatives. Its unique structure and functional groups provide insights into the mechanisms of various chemical reactions and contribute to the advancement of synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 849934-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,9,3 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849934-85:
(8*8)+(7*4)+(6*9)+(5*9)+(4*3)+(3*4)+(2*8)+(1*5)=236
236 % 10 = 6
So 849934-85-6 is a valid CAS Registry Number.

849934-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [6-ethoxy-5-(trifluoromethyl)pyridin-3-yl]boronic acid

1.2 Other means of identification

Product number -
Other names 6-ethoxy-5-(trifluoromethyl)pyridin-3-ylboronic acid

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:849934-85-6 SDS

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