871826-12-9 Usage
Uses
Used in Pharmaceutical and Medicinal Chemistry:
2-(Aminomethyl)-5-(trifluoromethyl)pyridine hydrochloride is utilized as a building block for the synthesis of various organic molecules with potential applications in drug discovery. Its unique structure and functional groups contribute to the development of new pharmaceutical agents.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2-(Aminomethyl)-5-(trifluoromethyl)pyridine hydrochloride serves as a reagent, facilitating the creation of complex organic compounds for a range of applications.
Used in Biological Research:
2-(Aminomethyl)-5-(trifluoromethyl)pyridine hydrochloride is employed as a molecular probe in biological research, aiding in the investigation of biological processes and the discovery of new therapeutic targets.
Used in Drug Candidate Development:
Due to its potential biological and pharmacological properties, 2-(Aminomethyl)-5-(trifluoromethyl)pyridine hydrochloride is studied for its role as a drug candidate, with the aim of advancing novel treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 871826-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,8,2 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 871826-12:
(8*8)+(7*7)+(6*1)+(5*8)+(4*2)+(3*6)+(2*1)+(1*2)=189
189 % 10 = 9
So 871826-12-9 is a valid CAS Registry Number.
871826-12-9Relevant academic research and scientific papers
Preparation method of 2-aminomethyl-5-trifluoromethylpyridinium salt
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Paragraph 0019; 0033-0035; 0039-0041, (2020/06/17)
The invention discloses a preparation method of 2-aminomethyl-5-trifluoromethylpyridinium salt, and belongs to the technical field of pesticides and medical intermediates. According to the method, 2-cyano-3-chloro-5-trifluoromethylpyridine is taken as a raw material, hydrogenation is carried out in an alcohol solvent and an acid in the presence of a metal catalyst, molecular dechlorination is carried out while nitrile group hydrogenation is carried out, and the product 2-aminomethyl-5-trifluoromethylpyridinium salt is obtained after treatment. The method has the advantages of reasonable technical route selection, short reaction steps, mild reaction conditions, low raw material cost and high separation yield, and is suitable for industrial amplification.
