856834-88-3 Usage
Uses
Used in Pharmaceutical Industry:
2-(2-BROMOETHYL)-6-METHYLPYRIDINE is used as a building block for the synthesis of pharmaceuticals due to its chemical properties and reactivity, which make it an important intermediate in the production of various fine chemicals.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2-(2-BROMOETHYL)-6-METHYLPYRIDINE is utilized as a key component in the creation of various organic compounds, contributing to the development of new agrochemical products.
Used in Organic Synthesis:
2-(2-BROMOETHYL)-6-METHYLPYRIDINE is used as a versatile intermediate in organic synthesis for the preparation of a wide range of chemical compounds, leveraging its unique structural features and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 856834-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,8,3 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 856834-88:
(8*8)+(7*5)+(6*6)+(5*8)+(4*3)+(3*4)+(2*8)+(1*8)=223
223 % 10 = 3
So 856834-88-3 is a valid CAS Registry Number.
856834-88-3Relevant academic research and scientific papers
Radical Hydroarylation of Functionalized Olefins and Mechanistic Investigation of Photocatalytic Pyridyl Radical Reactions
Seath, Ciaran P.,Vogt, David B.,Xu, Zihao,Boyington, Allyson J.,Jui, Nathan T.
supporting information, p. 15525 - 15534 (2018/11/23)
We report the photoredox alkylation of halopyridines using functionalized alkene and alkyne building blocks. Selective single-electron reduction of the halogenated pyridines provides the corresponding heteroaryl radicals, which undergo anti-Markovnikov addition to the alkene substrates. The system is shown to be mild and tolerant of a variety of alkene and alkyne subtypes. A combination of computational and experimental studies support a mechanism involving proton-coupled electron transfer followed by medium-dependent alkene addition and rapid hydrogen atom transfer mediated by a polarity-reversal catalyst.
