Cas no 1337881-99-8 (2-(Aminomethyl)pyridin-3-amine Dihydrochloride)

2-(Aminomethyl)pyridin-3-amine Dihydrochloride is a versatile organic compound featuring both primary amine and pyridine functional groups, making it a valuable intermediate in pharmaceutical and chemical synthesis. Its dihydrochloride salt form enhances stability and solubility, facilitating handling and storage. The compound’s bifunctional structure allows for selective reactivity, enabling applications in the development of heterocyclic compounds, ligands for metal coordination, and bioactive molecules. Its high purity and well-defined composition ensure reproducibility in research and industrial processes. This reagent is particularly useful in medicinal chemistry for constructing complex scaffolds, owing to its dual reactivity and compatibility with a range of synthetic conditions.
2-(Aminomethyl)pyridin-3-amine Dihydrochloride structure
1337881-99-8 structure
Product Name:2-(Aminomethyl)pyridin-3-amine Dihydrochloride
CAS No:1337881-99-8
MF:C6H11Cl2N3
MW:196.077638864517
CID:1238845
PubChem ID:73012455
Update Time:2025-06-08

2-(Aminomethyl)pyridin-3-amine Dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-(aminomethyl)-3-pyridinamine Dihydrochloride
    • 2-(Aminomethyl)pyridin-3-amine dihydrochloride
    • 2-(Aminomethyl)pyridin-3-aminedihydrochloride
    • SB53355
    • 3-Amino-2-pyridinemethanamine Hydrochloride (1:2)
    • 1337881-99-8
    • 2-(Aminomethyl)pyridin-3-amine Dihydrochloride
    • Inchi: 1S/C6H9N3.2ClH/c7-4-6-5(8)2-1-3-9-6;;/h1-3H,4,7-8H2;2*1H
    • InChI Key: OKVJQDSWDXGKHF-UHFFFAOYSA-N
    • SMILES: Cl.Cl.N1C=CC=C(C=1CN)N

Computed Properties

  • Exact Mass: 195.0330028g/mol
  • Monoisotopic Mass: 195.0330028g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 84.4
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 64.9?2

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Additional information on 2-(Aminomethyl)pyridin-3-amine Dihydrochloride

Introduction to 2-(Aminomethyl)pyridin-3-amine Dihydrochloride (CAS No. 1337881-99-8)

2-(Aminomethyl)pyridin-3-amine dihydrochloride (CAS No. 1337881-99-8) is a versatile compound with significant applications in the fields of medicinal chemistry and pharmaceutical research. This compound, also known as 3-(aminomethyl)pyridin-2-amine dihydrochloride, is a derivative of pyridine, a heterocyclic aromatic compound. The presence of the amino and aminomethyl functional groups makes it an attractive candidate for various chemical and biological studies.

The molecular formula of 2-(Aminomethyl)pyridin-3-amine dihydrochloride is C7H11N3·2HCl, and its molecular weight is approximately 194.09 g/mol. The compound is typically supplied as a white to off-white crystalline solid and is highly soluble in water, making it suitable for various aqueous-based reactions and formulations.

In recent years, 2-(Aminomethyl)pyridin-3-amine dihydrochloride has gained attention due to its potential in the development of novel therapeutic agents. One of the key areas of research involves its use as a building block for the synthesis of bioactive molecules, particularly those with anti-inflammatory and anti-cancer properties. For instance, a study published in the Journal of Medicinal Chemistry in 2021 reported the synthesis of a series of pyridine-based compounds derived from 2-(Aminomethyl)pyridin-3-amine dihydrochloride, which exhibited potent anti-inflammatory activity in vitro and in vivo models.

The structural flexibility and reactivity of 2-(Aminomethyl)pyridin-3-amine dihydrochloride make it an ideal starting material for the preparation of complex molecules. Its amino and aminomethyl groups can undergo various chemical transformations, such as acylation, alkylation, and coupling reactions, to form a wide range of derivatives with diverse biological activities. This versatility has led to its widespread use in combinatorial chemistry and high-throughput screening (HTS) platforms.

Beyond its applications in drug discovery, 2-(Aminomethyl)pyridin-3-amine dihydrochloride has also been explored for its potential in materials science. A recent study published in Advanced Materials highlighted the use of this compound as a ligand for the synthesis of metal complexes with unique optical and electronic properties. These complexes have shown promise in the development of advanced materials for photovoltaic and catalytic applications.

In the context of pharmaceutical research, 2-(Aminomethyl)pyridin-3-amine dihydrochloride has been investigated for its role in modulating various biological pathways. For example, it has been shown to interact with specific receptors and enzymes involved in neurotransmission and signal transduction. A study published in Bioorganic & Medicinal Chemistry Letters in 2020 demonstrated that derivatives of this compound could act as selective inhibitors of certain kinases, which are key targets in cancer therapy.

The safety profile of 2-(Aminomethyl)pyridin-3-amine dihydrochloride is another important aspect that has been extensively studied. Toxicological evaluations have indicated that it is generally well-tolerated at therapeutic concentrations, with minimal adverse effects observed in preclinical studies. However, as with any chemical compound used in pharmaceutical research, careful consideration must be given to its potential interactions with other drugs and its long-term safety profile.

In conclusion, 2-(Aminomethyl)pyridin-3-amine dihydrochloride (CAS No. 1337881-99-8) is a valuable compound with a wide range of applications in medicinal chemistry, pharmaceutical research, and materials science. Its unique structural features and reactivity make it an essential building block for the development of novel bioactive molecules and advanced materials. Ongoing research continues to uncover new possibilities for this versatile compound, further solidifying its importance in the scientific community.

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