870718-06-2 Usage
Uses
Used in Organic Synthesis:
2,4-DIFLUORO-3-FORMYLPHENYLBORONIC ACID is used as a reagent in organic synthesis for the preparation of various organic compounds. Its unique structure allows for the creation of a wide range of chemical entities, making it a valuable asset in the field of chemistry.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2,4-DIFLUORO-3-FORMYLPHENYLBORONIC ACID is utilized as a key intermediate in the synthesis of biologically active compounds. Its presence in the molecular structure can impart specific properties to the final product, contributing to the development of effective drugs.
Used in Agrochemical Development:
2,4-DIFLUORO-3-FORMYLPHENYLBORONIC ACID also finds application in the agrochemical sector, where it is employed in the synthesis of compounds with pesticidal or herbicidal properties. Its ability to be modified and incorporated into complex molecules makes it a promising candidate for the creation of novel agrochemicals.
Used in Research and Development:
2,4-DIFLUORO-3-FORMYLPHENYLBORONIC ACID is of significant interest to researchers in both the chemical and pharmaceutical industries. It is often used in experimental settings to explore new synthetic pathways, understand its reactivity, and evaluate its potential in various applications, including drug discovery and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 870718-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,7,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 870718-06:
(8*8)+(7*7)+(6*0)+(5*7)+(4*1)+(3*8)+(2*0)+(1*6)=182
182 % 10 = 2
So 870718-06-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BF2O3/c9-6-2-1-5(8(12)13)7(10)4(6)3-11/h1-3,12-13H
870718-06-2Relevant academic research and scientific papers
Functionalization of dihalophenylboronic acids by deprotonation of their N-butyldiethanolamine esters
Durka, Krzysztof,Kurach, Pawel,Lulinski, Sergiusz,Serwatowski, Janusz
experimental part, p. 4325 - 4332 (2011/02/22)
Deprotonative lithiation of various 6-butyl-2-(dihalophenyl)-(N-B)-1,3,6,2- dioxazaborocanes (N-butyldiethanolamine esters of dihalophenylboronic acids) was investigated. It was found that selective transformations can be best achieved by use of LDA as the lithiating reagent. The reactivities of these compounds vary significantly, depending on the natures and positions of the halogen atoms. The resultant boron-lithium bimetallic intermediates were subjected to reactions with electrophiles to afford functionalized halogenated arylboronic acids.
