Cas no 1171321-50-8 (Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride)

Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride is a chemically stable, high-purity compound primarily used in pharmaceutical and organic synthesis applications. Its dihydrochloride salt form enhances solubility in aqueous and polar solvents, facilitating its use in reaction systems requiring precise stoichiometry. The pyridinyl-ethylamine backbone serves as a versatile intermediate for constructing complex molecules, particularly in the development of bioactive compounds. The product is characterized by consistent batch-to-batch reproducibility and meets stringent analytical standards (e.g., HPLC, NMR). Its hygroscopic nature necessitates proper storage under inert conditions. Suitable for research-scale and industrial applications, it offers reliable performance in nucleophilic substitutions, reductive aminations, and catalyst preparations.
Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride structure
1171321-50-8 structure
Product Name:Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride
CAS No:1171321-50-8
MF:C8H14Cl2N2
MW:209.116159915924
CID:4574761
PubChem ID:42921612
Update Time:2025-10-29

Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • methyl[1-(pyridin-3-yl)ethyl]amine dihydrochloride
    • methyl[1-(pyridin-3-yl)ethyl]aminedihydrochloride
    • N-methyl-1-pyridin-3-ylethanamine;dihydrochloride
    • EN300-44074
    • 1171321-50-8
    • AKOS026726374
    • Z451350188
    • CS-0249604
    • Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride
    • Inchi: 1S/C8H12N2.2ClH/c1-7(9-2)8-4-3-5-10-6-8;;/h3-7,9H,1-2H3;2*1H
    • InChI Key: LBCWYZLEFPTFTN-UHFFFAOYSA-N
    • SMILES: N(C)C(C1=CC=CN=C1)C.[H]Cl.[H]Cl

Computed Properties

  • Exact Mass: 208.0534038g/mol
  • Monoisotopic Mass: 208.0534038g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 93.3
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 24.9?2

Experimental Properties

  • Melting Point: 247-249 °C

Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride Security Information

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Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride Related Literature

Additional information on Methyl1-(pyridin-3-yl)ethylamine Dihydrochloride

Methyl 1-(pyridin-3-yl)ethylamine Dihydrochloride: A Comprehensive Overview

Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride, also known by its CAS number CAS No. 1171321-50-8, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound is characterized by its unique structure, which combines a pyridine ring with an ethylamine group and a methyl substituent, all of which contribute to its diverse chemical properties and potential applications.

The molecular structure of Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride plays a crucial role in its reactivity and functionality. The pyridine ring, a six-membered aromatic ring with one nitrogen atom, imparts aromatic stability and electronic properties that are essential for various chemical reactions. The ethylamine group introduces nucleophilic character, making the compound amenable to reactions such as alkylation and acylation. Furthermore, the methyl substituent at the 3-position of the pyridine ring adds steric effects and influences the overall electronic distribution of the molecule.

Recent studies have highlighted the potential of Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride in drug discovery and development. Researchers have explored its role as a building block in synthesizing bioactive molecules, particularly those with potential therapeutic applications. For instance, derivatives of this compound have shown promise in targeting specific enzymes and receptors involved in diseases such as cancer and neurodegenerative disorders.

In addition to its role in drug development, Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride has been utilized in various chemical synthesis pathways. Its ability to act as both a nucleophile and an electrophile makes it versatile in forming different types of bonds, including C-N and C-C bonds. This versatility has led to its application in the synthesis of complex molecules, such as natural product analogs and advanced materials.

The synthesis of Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride typically involves multi-step processes that require precise control over reaction conditions. Key steps often include nucleophilic substitution reactions, reductions, and acid-base neutralizations. The use of modern synthetic techniques, such as microwave-assisted synthesis and catalytic methods, has significantly improved the efficiency and yield of these processes.

From an analytical standpoint, the characterization of Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride relies on advanced spectroscopic methods such as NMR (nuclear magnetic resonance), IR (infrared spectroscopy), and MS (mass spectrometry). These techniques provide detailed insights into the molecular structure, purity, and stability of the compound. Recent advancements in analytical chemistry have further enhanced our ability to accurately determine the physical and chemical properties of this compound.

In terms of applications, Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride has found utility in diverse fields beyond pharmacology. For example, it has been employed in materials science for the development of novel polymers and coatings with tailored properties. Its ability to form stable complexes with metal ions has also made it a valuable reagent in coordination chemistry.

The environmental impact of Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride is another area of growing interest. Researchers are investigating its biodegradability, toxicity, and potential ecological effects to ensure sustainable practices in its production and use. This focus on environmental considerations aligns with global efforts to promote green chemistry principles across various industries.

In conclusion, Methyl 1-(pyridin-3-yl)ethylamine dihydrochloride, CAS No. 1171321-50-8, is a multifaceted compound with significant implications across multiple disciplines. Its unique chemical properties, versatile applications, and ongoing research into its potential uses make it a subject of continued scientific interest. As advancements in chemistry continue to unfold, this compound is likely to play an increasingly important role in both academic research and industrial applications.

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