32399-08-9 Usage
Uses
Used in Organic Synthesis:
2-Methylaminopyridine-3-carbaldehyde is used as a building block for its ability to engage in various chemical reactions, facilitating the creation of complex organic molecules and contributing to the advancement of organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Methylaminopyridine-3-carbaldehyde is utilized as a key component in the synthesis of biologically active compounds. Its unique properties and reactivity make it instrumental in the development of new drugs, enhancing the discovery and innovation of therapeutic agents.
Used in Drug Development:
2-Methylaminopyridine-3-carbaldehyde is employed in the development of new drugs due to its potential to form a variety of biologically active molecules. Its role in medicinal chemistry is crucial for the creation of novel pharmaceuticals that address unmet medical needs.
Used as a Reagent in Organic Chemistry:
2-Methylaminopyridine-3-carbaldehyde also serves as a reagent in organic chemistry, where its reactivity is harnessed to facilitate specific chemical transformations and reactions, thereby aiding in the synthesis of target molecules and the study of reaction mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 32399-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,9 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32399-08:
(7*3)+(6*2)+(5*3)+(4*9)+(3*9)+(2*0)+(1*8)=119
119 % 10 = 9
So 32399-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O/c1-8-7-6(5-10)3-2-4-9-7/h2-5H,1H3,(H,8,9)
32399-08-9Relevant academic research and scientific papers
Ring Opening and Transamination of Pyridinium Salts
Fadda, A. A.,Abdelrazek, F. M.,El-Habbal, M. M.
, p. 194 - 195 (2007/10/02)
N-Alkyl-3-cyanopyridinium iodides (Ia-c) undergo ring opening and recyclization when heated with aq. alkyl amine to give 2-alkylamino-3-formylpyridines (IIa-c) and 3-cyanopyridine (III).However, when compounds Ia-c are treated with alkyl amines in which t
COVALENT ADDUCTS FROM 1,3-DISUBSTITUTED PYRIDINIUM SALTS AND PIPERIDINE
Moracci, F. Micheletti,Rienzo, B. Di,Tortorella, S.,Liberatore, F.
, p. 785 - 789 (2007/10/02)
Covalent adducts 3a-f have been isolated from the reaction between piperidine and pyridinium salts 1a-f. 3a-f are stable both in the solid state and in apolar solvents, whereas their fast dissociation back to piperidine and pyridinium ions occurs in aqueous solution.The latter, in the alkaline environment produced by the amine, yields the correspondent pseudobases, which are key intermediates of the subsequent reactions.For instance, the pseudobases from 1a,b can undergo either a ring-opening reaction or a redox process with the corresponding pyridinium cations.
