3510-66-5 Usage
Description
2-Bromo-5-methylpyridine is an organic compound characterized by its light brown solid appearance. It is a derivative of pyridine, a heterocyclic aromatic compound, with a bromine atom at the 2nd position and a methyl group at the 5th position. 2-Bromo-5-methylpyridine is known for its chemical reactivity and is commonly utilized as a building block in the synthesis of various complex organic molecules, particularly those with potential applications in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Industry:
2-Bromo-5-methylpyridine is used as a key intermediate in the preparation of [[(triazolylmethyl)pyridyl]phenyl]tetrazoles and related compounds. These compounds are of significant interest due to their potential as cardiovascular agents, which can be used in the development of new drugs to treat heart-related conditions.
Used in Chemical Synthesis:
Check Digit Verification of cas no
The CAS Registry Mumber 3510-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3510-66:
(6*3)+(5*5)+(4*1)+(3*0)+(2*6)+(1*6)=65
65 % 10 = 5
So 3510-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrN/c1-5-2-3-6(7)8-4-5/h2-4H,1H3
3510-66-5Relevant articles and documents
PROCESS FOR THE PREPARATION OF ABAMETAPIR AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS
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Page/Page column 13, (2019/10/04)
The present invention relates to process for the preparation of Abametapir. The present 5 invention further relates to Abametapir salts and their preparation thereof.
Direct Transformation of Arylamines to Aryl Halides via Sodium Nitrite and N-Halosuccinimide
Mukhopadhyay, Sushobhan,Batra, Sanjay
supporting information, p. 14622 - 14626 (2018/09/21)
A one-pot universal approach for transforming arylamines to aryl halides via reaction with sodium nitrite (NaNO2) and N-halosuccinimide (NXS) in DMF at room temperature under metal- and acid-free condition is described. This new protocol that is complementary to the Sandmeyer reaction, is suggested to involve the in situ generation of nitryl halide induce nitrosylation of aryl amine to form the diazo intermediate which is halogenated to furnish the aryl halide.
2,6-DIOXO,-2,3-DIHYDRO-1H-PURINE COMPOUNDS USEFUL FOR TREATING DISORDERS RELATED TO THE ACTIVITY OF THE TRPA1 CHANNEL
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Paragraph 0624, (2017/07/14)
Compounds of formula (VIII) and compositions for treating disorders related to TRPA1 are described herein.