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4-FLUORO-2-HYDROXYPHENYLBORONIC ACID is a chemical compound with the molecular formula C6H6BFO3. It is a boronic acid derivative featuring a fluorine atom and a hydroxy group attached to a phenyl ring. 4-FLUORO-2-HYDROXYPHENYLBORONIC ACID is recognized for its versatility in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to form carbon-carbon and carbon-heteroatom bonds positions it as a crucial reagent in medicinal chemistry and chemical research. Additionally, as a boronic acid, it can form stable complexes with diols, which is beneficial for the synthesis of glycoconjugates and glycomimetics.

850568-00-2

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850568-00-2 Usage

Uses

Used in Pharmaceutical Industry:
4-FLUORO-2-HYDROXYPHENYLBORONIC ACID is used as a building block for the synthesis of various pharmaceuticals due to its capacity to form essential chemical bonds and its compatibility with a range of chemical reactions in drug development.
Used in Agrochemical Industry:
In the agrochemical sector, 4-FLUORO-2-HYDROXYPHENYLBORONIC ACID is utilized as a key component in the creation of agrochemicals, leveraging its reactivity to produce compounds with pesticidal or herbicidal properties.
Used in Advanced Materials:
4-FLUORO-2-HYDROXYPHENYLBORONIC ACID is employed as a precursor in the development of advanced materials, where its unique structure and bonding capabilities contribute to the creation of new materials with specialized properties.
Used in Medicinal Chemistry Research:
As a versatile reagent, 4-FLUORO-2-HYDROXYPHENYLBORONIC ACID is used in medicinal chemistry research for the formation of carbon-carbon and carbon-heteroatom bonds, which are fundamental in the synthesis of complex organic molecules with potential therapeutic applications.
Used in the Synthesis of Glycoconjugates and Glycomimetics:
4-FLUORO-2-HYDROXYPHENYLBORONIC ACID is used as a reagent for the synthesis of glycoconjugates and glycomimetics, taking advantage of its ability to form stable complexes with diols, which is essential in the construction of these complex carbohydrate-containing molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 850568-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 850568-00:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*8)+(2*0)+(1*0)=172
172 % 10 = 2
So 850568-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BFO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9-11H

850568-00-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H53304)  4-Fluoro-2-hydroxybenzeneboronic acid, 97%   

  • 850568-00-2

  • 250mg

  • 1042.0CNY

  • Detail
  • Alfa Aesar

  • (H53304)  4-Fluoro-2-hydroxybenzeneboronic acid, 97%   

  • 850568-00-2

  • 1g

  • 3334.0CNY

  • Detail

850568-00-2SDS

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 (4-fluoro-2-hydroxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-Fluoro-2-hydroxybenzeneboronic 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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:850568-00-2 SDS

850568-00-2Relevant academic research and scientific papers

Phenolate substituent effects on ring-opening polymerization of ε-caprolactone by aluminum complexes bearing 2-(phenyl-2-olate)-6-(1- amidoalkyl)pyridine pincers

Alkarekshi, Wafaa,Armitage, Andrew P.,Boyron, Olivier,Davies, Christopher J.,Govere, Matifadza,Gregory, Andrew,Singh, Kuldip,Solan, Gregory A.

, p. 249 - 259 (2013/02/25)

Interaction of the 2-(phenyl-2-ol)-6-ketiminopyridines 2-(4′-R 1-C6H3-2′-OH)-6-{CMe=N(2″,6″- i-Pr2C6H3)}C5H3N (R 1 = H (L1a-H), But (L

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