166316-48-9 Usage
Description
4-(2-Carboxyethyl)benzeneboronic acid is an organic compound characterized by its boronic acid functional group and a carboxyethyl side chain attached to a benzene ring. This molecule exhibits unique chemical properties due to the presence of both the boronic acid and carboxylic acid groups, making it a versatile intermediate in various chemical syntheses and applications.
Uses
Used in Agrochemical Industry:
4-(2-Carboxyethyl)benzeneboronic acid is used as an intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its unique chemical properties allow for the development of new compounds with improved efficacy and selectivity in controlling pests and weeds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(2-Carboxyethyl)benzeneboronic acid serves as a key intermediate in the development of new drugs. Its ability to form stable complexes with biological targets, such as enzymes and receptors, makes it a valuable component in the design of novel therapeutic agents.
Used in Dyestuff Industry:
4-(2-Carboxyethyl)benzeneboronic acid is also utilized in the dyestuff industry for the production of various dyes and pigments. Its chemical structure contributes to the color properties and stability of the resulting dyes, making it an important component in the formulation of colorants for various applications, including textiles, plastics, and inks.
Check Digit Verification of cas no
The CAS Registry Mumber 166316-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,3,1 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 166316-48:
(8*1)+(7*6)+(6*6)+(5*3)+(4*1)+(3*6)+(2*4)+(1*8)=139
139 % 10 = 9
So 166316-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H11BO4/c11-9(12)6-3-7-1-4-8(5-2-7)10(13)14/h1-2,4-5,13-14H,3,6H2,(H,11,12)
166316-48-9Relevant articles and documents
Syntheses with organoboranes. XIII. Synthesis of ω-(4-bromophenyl)alkanoic acids and their borylation
Zaidlewicz, Marek,Wolan, Andrzej
, p. 129 - 135 (2007/10/03)
ω-(4-Bromophenyl)alkanoic acids 2c-e were obtained from 1-bromo-4-alkenylbenzenes 5c-e by hydroboration-thermal isomerization-oxidation. Their esters 11c-e were transformed in good yields into the corresponding boronates 12c-e by the cross-coupling reaction with (10) in an ionic liquid, [bmim][BF4]. The use of pinacolborane for the coupling reaction in the ionic liquid gave debromination products, and low yields of 12c-e. Ethyl 3-(4-bromophenyl)propanoate (7c) was transformed into ethyl 3-(4-[1,3,2]dioxaborolanyl)propanoate (9c) by the cross-coupling with [2,2′]bi[[1,3,2]dioxaborinanyl].
