148562-12-3 Usage
Description
6-Bromohexylboronic acid is an organic compound that features a boron atom bonded to a hydrocarbon chain with a bromine atom at the sixth position. It is a versatile reagent in organic synthesis and has various applications in different industries due to its unique chemical properties.
Uses
Used in Chemical Synthesis:
6-Bromohexylboronic acid is used as a substrate in the radical alkylation reactions of boronic acids using organic photocatalysts. This application takes advantage of its reactivity under specific conditions to form new compounds with potential applications in various fields.
Used in Pharmaceutical Industry:
6-Bromohexylboronic acid is used as a substrate in the Ag(I) catalyzed difluoromethylthiolation of various boronic acids using S-(difluoromethyl) benzenesulfonothioate. This reaction is significant in the synthesis of pharmaceutical compounds, as it can introduce a difluoromethylthio group into the molecule, which may enhance the biological activity or pharmacokinetic properties of the resulting compound.
Used in Analytical Chemistry:
6-Bromohexylboronic acid serves as a starting material in the synthesis of fluorescent carbon nanodots. These nanodots are applicable in the estimation of tannic acid in wine samples, providing a sensitive and selective method for detecting and quantifying this important compound in the beverage industry.
Check Digit Verification of cas no
The CAS Registry Mumber 148562-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,5,6 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148562-12:
(8*1)+(7*4)+(6*8)+(5*5)+(4*6)+(3*2)+(2*1)+(1*2)=143
143 % 10 = 3
So 148562-12-3 is a valid CAS Registry Number.
148562-12-3Relevant articles and documents
Visible-Light-Induced C2 Alkylation of Pyridine N-Oxides
Zhang, Wen-Man,Dai, Jian-Jun,Xu, Jun,Xu, Hua-Jian
, p. 2059 - 2066 (2017/02/26)
A photoredox catalytic method has been developed for the direct C2 alkylation of pyridine N-oxides. This reaction is compatible with a range of synthetically relevant functional groups for providing efficient synthesis of a variety of C2-alkylated pyridine N-oxides under mild conditions. Mechanistic studies are consistent with the generation of a radical intermediate along the reaction pathway.
