852181-11-4 Usage
Uses
Used in Pharmaceutical Industry:
2,5-Dibromonicotinaldehyde is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to participate in a range of chemical reactions that facilitate the creation of new drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 2,5-Dibromonicotinaldehyde is utilized as a reagent in the production of agrochemicals, contributing to the development of compounds that can enhance crop protection and yield.
Used in Specialty Chemicals Production:
2,5-Dibromonicotinaldehyde is employed as a reagent in the synthesis of specialty chemicals, where its unique properties are leveraged to create complex and highly specific chemical entities for various applications.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2,5-Dibromonicotinaldehyde is used for the formation of heterocyclic compounds and the modification of organic molecules, playing a crucial role in advancing the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 852181-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,1,8 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 852181-11:
(8*8)+(7*5)+(6*2)+(5*1)+(4*8)+(3*1)+(2*1)+(1*1)=154
154 % 10 = 4
So 852181-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Br2NO/c7-5-1-4(3-10)6(8)9-2-5/h1-3H
852181-11-4Relevant academic research and scientific papers
HETEROCYCLIC CGRP RECEPTOR ANTAGONISTS
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Page/Page column 38, (2016/05/11)
The present invention is directed to heterocyclic compounds which are antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which CGRP is involved, such as migraine. The invention is also directed to pharmaceutical composi
Synthesis of new [2,3′:6′,3″]terpyridines using iterative cross-coupling reactions
Burzicki, Gregory,Voisin-Chiret, Anne Sophie,Santos, Jana Sopkova-De Oliveira,Rault, Sylvain
experimental part, p. 2804 - 2810 (2010/10/19)
An efficient, regioselective, and global route to prepare terpyridines is described. A predictable strategy was developed, which is based on iterative cross-coupling reactions between bifunctional pyridylboronic acids as promising platforms and halobipyridines as key intermediates. Georg Thieme Verlag Stuttgart.
