6-Bromo-3-fluoro-2-ethoxyphenylboronic acid is a boronic acid derivative characterized by the molecular formula C8H10BBrFO3. It features a phenyl ring with a bromine atom at the 6th position, a fluoro atom at the 3rd position, and an ethoxy group at the 2nd position. This chemical compound is known for its versatile reactivity and applications in various fields.
1310403-98-5
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Basic information
- Product Name: 6-Bromo-3-fluoro-2-ethoxyphenylboronic acid
- Synonyms: 6-Bromo-3-fluoro-2-ethoxyphenylboronic acid;(6-Bromo-2-ethoxy-3-fluorophenyl)
- CAS NO:1310403-98-5
- Molecular Formula: C8H9BBrFO3
- Molecular Weight: 262.88
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1310403-98-5.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
- Solubility: N/A
- CAS DataBase Reference: 6-Bromo-3-fluoro-2-ethoxyphenylboronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: 6-Bromo-3-fluoro-2-ethoxyphenylboronic acid(1310403-98-5)
- EPA Substance Registry System: 6-Bromo-3-fluoro-2-ethoxyphenylboronic acid(1310403-98-5)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1310403-98-5(Hazardous Substances Data)
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1310403-98-5 Usage
Uses
Used in Organic Synthesis:6-Bromo-3-fluoro-2-ethoxyphenylboronic acid is used as a building block in organic synthesis for the creation of biologically active molecules, pharmaceuticals, and agrochemicals. Its unique structure allows for the formation of carbon-carbon bonds through cross-coupling reactions, such as Suzuki coupling, facilitating the synthesis of complex organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-Bromo-3-fluoro-2-ethoxyphenylboronic acid is utilized as a key intermediate in the synthesis of various drug molecules. Its ability to participate in cross-coupling reactions enables the development of new pharmaceutical agents with improved therapeutic properties and reduced side effects.
Used in Agrochemical Industry:
6-Bromo-3-fluoro-2-ethoxyphenylboronic acid is employed as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity in cross-coupling reactions allows for the development of novel agrochemicals with enhanced efficacy and selectivity, contributing to more sustainable agricultural practices.
Used as a Ligand in Metal-Catalyzed Reactions:
6-Bromo-3-fluoro-2-ethoxyphenylboronic acid's boronic acid functionality makes it a valuable ligand in metal-catalyzed reactions. Its use in these reactions contributes to the development of new synthetic methods and the improvement of existing ones, expanding the scope of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 1310403-98-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,4,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.Calculate Digit Verification of CAS Registry Number 1310403-98:
(9*1)+(8*3)+(7*1)+(6*0)+(5*4)+(4*0)+(3*3)+(2*9)+(1*8)=95
95 % 10 = 5
So 1310403-98-5 is a valid CAS Registry Number.
1310403-98-5Upstream product
1310403-98-5Downstream Products
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6-Bromo-3-fluoro-2-ethoxyphenylboronic acid
