352535-82-1 Usage
Description
3-CHLORO-2-FLUOROPHENYLBORONIC ACID is an organic compound that features a boronic acid functional group attached to a phenyl ring substituted with a chlorine atom at the 3rd position and a fluorine atom at the 2nd position. This unique structure endows it with versatile reactivity and properties, making it a valuable building block in various chemical and biological applications.
Uses
Used in Inorganic Synthesis:
3-CHLORO-2-FLUOROPHENYLBORONIC ACID is used as a synthetic building block for the creation of complex inorganic compounds. Its unique structure allows for selective functionalization and the formation of diverse chemical entities.
Used in Catalysis:
In the field of catalysis, 3-CHLORO-2-FLUOROPHENYLBORONIC ACID serves as a catalyst or a catalyst precursor, facilitating various chemical reactions with improved efficiency and selectivity.
Used in Analytical Chemistry:
3-CHLORO-2-FLUOROPHENYLBORONIC ACID is employed as a reagent or a derivatizing agent in analytical chemistry, enabling the detection, identification, and quantification of specific compounds or functional groups.
Used in Biological Systems:
In the realm of biology, 3-CHLORO-2-FLUOROPHENYLBORONIC ACID is utilized as a molecular probe or a building block for the development of bioactive molecules, targeting various biological processes and pathways.
Used in Pharmaceutical Industry:
3-CHLORO-2-FLUOROPHENYLBORONIC ACID is used as a key intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Material Science:
In material science, 3-CHLORO-2-FLUOROPHENYLBORONIC ACID is used as a component in the design and synthesis of novel materials with specific properties, such as improved conductivity, stability, or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 352535-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 352535-82:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*8)+(1*2)=141
141 % 10 = 1
So 352535-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BClFO2/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,10-11H
352535-82-1Relevant articles and documents
HETEROCYCLIC COMPOUND, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE
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Paragraph 0208; 0209; 0210, (2015/03/16)
A novel heterocyclic compound that can be used as a host material in which a light-emitting substance is dispersed. A light-emitting element having a long lifetime. A heterocyclic compound in which a substituted or unsubstituted dibenzo[f,h]quinoxalinyl group is bonded to a substituted or unsubstituted arylene group having 6 to 25 carbon atoms which is bonded to any one of the 8-11 positions of a substituted or unsubstituted benzo[b]naphtho[1,2-d]furan skeleton.
HETEROCYCLIC COMPOUND, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE
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Paragraph 0274; 0275; 0276, (2014/05/24)
To provide a novel heterocyclic compound capable of being used as a host material in which a light-emitting substance is dispersed. To provide a light-emitting element having a long lifetime. A heterocyclic compound in which a dibenzo[f,h]quinoxalinyl group and a benzo[b]naphtho[1,2-d]furanyl group are bonded through an arylene group having 6 to 13 carbon atoms. The dibenzo[f,h]quinoxalinyl group, the benzo[b]naphtho[1,2-d]furanyl group, and the arylene group separately are unsubstituted or have, as a substituent, an alkyl group having 1 to 4 carbon atoms or an aryl group having 6 to 13 carbon atoms.
General method for the synthesis of substituted phenanthridin-6(5H)-ones using a KOH-mediated anionic ring closure as the key step
Dubost, Emmanuelle,Magnelli, Rosa,Cailly, Thomas,Legay, Rémi,Fabis, Frédéric,Rault, Sylvain
experimental part, p. 5008 - 5016 (2010/08/13)
Substituted phenanthridin-6(5H)-ones were obtained in a two-step procedure involving a Suzuki cross-coupling reaction followed by a KOH-mediated anionic ring closure. The influence of the nature and the position of the substituents on the cyclization step were studied. This methodology offers a general and practical route to diversely substituted phenanthridin-6(5H)-ones.