Cas no 1965308-99-9 (5-Aminopyrazine-2-carbaldehyde hydrochloride)

5-Aminopyrazine-2-carbaldehyde hydrochloride is a versatile heterocyclic building block used in organic synthesis and pharmaceutical research. Its reactive aldehyde and amino groups enable efficient derivatization, making it valuable for constructing complex molecular frameworks, particularly in medicinal chemistry. The hydrochloride salt enhances stability and solubility, facilitating handling and storage. This compound is particularly useful in the synthesis of pyrazine-based scaffolds, which are prevalent in bioactive molecules and agrochemicals. Its high purity and well-defined structure ensure reproducibility in synthetic applications. Researchers favor it for its compatibility with a range of coupling and condensation reactions, supporting the development of novel compounds with potential therapeutic or industrial applications.
5-Aminopyrazine-2-carbaldehyde hydrochloride structure
1965308-99-9 structure
Product Name:5-Aminopyrazine-2-carbaldehyde hydrochloride
CAS No:1965308-99-9
MF:C5H6ClN3O
MW:159.573639392853
MDL:MFCD30181953
CID:4710048
PubChem ID:124222617
Update Time:2025-05-23

5-Aminopyrazine-2-carbaldehyde hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 5-aminopyrazine-2-carbaldehyde hydrochloride
    • 5-Aminopyrazine-2-carbaldehyde HCl
    • SB34928
    • 1965308-99-9
    • 5-Amino-pyrazine-2-carbaldehydehydrochloride
    • CS-16658
    • 5-Amino-pyrazine-2-carbaldehyde HCl
    • AKOS030528318
    • F31178
    • SY263206
    • MFCD30181953
    • 5-aminopyrazine-2-carbaldehyde;hydrochloride
    • 5-Amino-pyrazine-2-carbaldehyde hydrochloride
    • CS-0102085
    • 5-aminopyrazine-2-carbaldehydehydrochloride
    • 5-Aminopyrazine-2-carbaldehyde hydrochloride
    • MDL: MFCD30181953
    • Inchi: 1S/C5H5N3O.ClH/c6-5-2-7-4(3-9)1-8-5;/h1-3H,(H2,6,8);1H
    • InChI Key: MSBFKKZIBSVAQS-UHFFFAOYSA-N
    • SMILES: Cl.O=CC1=CN=C(C=N1)N

Computed Properties

  • Exact Mass: 159.0199395g/mol
  • Monoisotopic Mass: 159.0199395g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 106
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 68.9

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Additional information on 5-Aminopyrazine-2-carbaldehyde hydrochloride

Comprehensive Overview of 5-Aminopyrazine-2-carbaldehyde hydrochloride (CAS No. 1965308-99-9)

5-Aminopyrazine-2-carbaldehyde hydrochloride (CAS No. 1965308-99-9) is a specialized organic compound widely utilized in pharmaceutical research and fine chemical synthesis. This compound, often referred to as a pyrazine derivative, has garnered significant attention due to its versatile applications in drug discovery and material science. Its molecular structure, featuring an aminopyrazine core and a carbaldehyde group, makes it a valuable intermediate for constructing complex molecules. Researchers and industries are increasingly exploring its potential in developing novel therapeutics and functional materials.

The growing interest in 5-Aminopyrazine-2-carbaldehyde hydrochloride aligns with current trends in precision medicine and green chemistry. As the demand for high-purity intermediates rises, this compound stands out for its role in synthesizing targeted therapies and biocompatible materials. Its CAS No. 1965308-99-9 is frequently searched in academic databases and chemical marketplaces, reflecting its relevance in modern research. Users often inquire about its synthetic routes, solubility profiles, and stability under various conditions, highlighting its practical importance.

From a structural perspective, 5-Aminopyrazine-2-carbaldehyde hydrochloride exhibits unique electronic properties due to its heterocyclic framework. This characteristic enables it to participate in diverse cross-coupling reactions and catalyzed transformations, making it a staple in medicinal chemistry. Recent studies have explored its utility in designing kinase inhibitors and antimicrobial agents, addressing pressing healthcare challenges. The compound's hydrochloride salt form enhances its handling and storage convenience, further boosting its adoption in laboratories.

In the context of SEO optimization, keywords such as "buy 5-Aminopyrazine-2-carbaldehyde hydrochloride," "CAS 1965308-99-9 suppliers," and "pyrazine aldehyde applications" are frequently queried. These long-tail keywords reflect user intent, ranging from procurement to technical inquiries. By addressing these topics, this article aims to provide a comprehensive resource for chemists, procurement specialists, and R&D professionals. Additionally, discussions on scalable synthesis methods and quality control standards resonate with industry stakeholders seeking reliable compound sources.

Looking ahead, 5-Aminopyrazine-2-carbaldehyde hydrochloride is poised to play a pivotal role in advancing personalized medicine and sustainable chemistry. Its integration into high-throughput screening platforms and catalyst design underscores its multidisciplinary appeal. As researchers uncover new applications, its CAS No. 1965308-99-9 will remain a focal point in scientific literature and commercial catalogs. This compound exemplifies the synergy between molecular innovation and industrial applicability, driving progress across multiple scientific domains.

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