872492-59-6 Usage
Description
(3-Bromo-5-Methyl-pyridin-2-yl)-Methyl-aMine, also known as 3-Bromo-5-methyl-2-picolinylamine, is a pyridine derivative with the molecular formula C7H8BrN3. (3-BroMo-5-Methyl-pyridin-2-yl)-Methyl-aMine features a bromine atom, a methyl group, and an amino group, making it a versatile chemical building block. Its unique structure and properties have attracted the attention of researchers in medicinal chemistry, chemical biology, and materials science due to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(3-Bromo-5-Methyl-pyridin-2-yl)-Methyl-aMine is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structure of various drugs. Its presence in the final product can enhance the drug's efficacy, selectivity, or stability.
Used in Agrochemical Industry:
In the agrochemical industry, (3-Bromo-5-Methyl-pyridin-2-yl)-Methyl-aMine is utilized as a building block for the development of new agrochemicals, such as pesticides and herbicides. Its incorporation can lead to improved performance and selectivity of these chemicals, benefiting agricultural practices.
Used in Organic Compounds Synthesis:
(3-Bromo-5-Methyl-pyridin-2-yl)-Methyl-aMine is also used as an intermediate in the synthesis of other organic compounds. Its unique functional groups allow for further chemical reactions, leading to the creation of a wide range of molecules with various applications in different industries.
Used in Chemical Biology Research:
As a compound with diverse functional groups, (3-Bromo-5-Methyl-pyridin-2-yl)-Methyl-aMine is valuable in chemical biology research. It can be used to study the interactions between small molecules and biological targets, potentially leading to the discovery of new bioactive molecules or the development of novel therapeutic strategies.
Overall, (3-Bromo-5-Methyl-pyridin-2-yl)-Methyl-aMine is a significant chemical intermediate with a broad spectrum of potential applications across the pharmaceutical, agrochemical, and materials science industries, as well as in research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 872492-59-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,4,9 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 872492-59:
(8*8)+(7*7)+(6*2)+(5*4)+(4*9)+(3*2)+(2*5)+(1*9)=206
206 % 10 = 6
So 872492-59-6 is a valid CAS Registry Number.
872492-59-6Relevant articles and documents
A valuable synthesis of pyrrolo[1,2-a]quinoxalines, indolo[1,2-a] quinoxalines and their aza-analogues by palladium-catalyzed intramolecular carbon-nitrogen bond formation
Abbiati, Giorgio,Beccalli, Egle M.,Broggini, Gianluigi,Paladino, Giuseppe,Rossi, Elisabetta
, p. 2881 - 2886 (2005)
A novel and efficient method for the construction of pyrrolo[1,2-a] quinoxalines, indolo[1,2-a]quinoxalines and their aza-analogues is described. The reaction involves a Pd-catalyzed intramolecular cyclization as the key step and provides the desired prod
