290832-43-8

Basic information

• Product Name: 2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID
• Synonyms: 2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID
• CAS NO: 290832-43-8
• Molecular Formula: C₈H₈BF₃O₄
• Molecular Weight: 235.95
• Product Categories: Aryl;Organoborons
• Mol File: 290832-43-8.mol

Chemical Properties

• Boiling Point: 324.549 ºCat 760 mmHg
• Flash Point: 150.082 ºC
• Appearance: /
• Density: 1.406
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.465
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID(290832-43-8)
• EPA Substance Registry System: 2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID(290832-43-8)

Safety Data

• Hazardous Substances Data: 290832-43-8(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID is used as a reagent in the Suzuki-Miyaura cross-coupling reaction for the formation of carbon-carbon bonds. This reaction is crucial in the synthesis of complex organic molecules, including pharmaceuticals and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID is utilized for the synthesis of various organic compounds that have potential medicinal properties. Its role in creating new chemical entities is vital for the development of novel drugs and therapeutic agents.
Used in Materials Science:
2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID is employed in materials science for the synthesis of organic compounds that can be used in the development of new materials with specific properties, such as improved conductivity, stability, or reactivity.
Used in Research and Development:
In the realm of research and development, 2-ISOPROPOXY-5-(TRIFLUOROMETHOXY)PHENYLBORONIC ACID is used as a key reagent for exploring new chemical reactions and mechanisms, contributing to the advancement of organic chemistry knowledge and its applications.

InChI:InChI=1/C8H8BF3O4/c1-15-7-3-2-5(16-8(10,11)12)4-6(7)9(13)14/h2-4,13-14H,1H3

Upstream product

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Downstream Products

• 895572-36-8 2-methoxy-5-(trifluoromethoxy)phenol 
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• 1354819-27-4 2-[3-nitro-1-(tetrahydro-2H-pyra-2-yl)-1H-pyrazol-4-yl]-4-(trifluoromethoxy)phenol 
• 1354819-28-5 tert-butyl [(5-chloro-2-fluoro-4-{2-[3-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-4-yl]-4-(trifluoromethoxy)phenoxy}phenyl)sulfonyl]1,3-thiazol-4-ylcarbamate 
• 200952-78-9 (5R,6S)-3-(2-Methoxy-5-trifluoromethoxy-phenyl)-6-phenyl-1-oxa-7-aza-spiro[4.5]dec-3-ene-7-carboxylic acid tert-butyl ester 

Relevant articles and documents

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