Cas no 1187931-12-9 (2-Chloro-pyrido2,3-bpyrazine Dihydrochloride)

2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride is a heterocyclic compound featuring a chloro-substituted pyridopyrazine core with two hydrochloride salt groups. This derivative is valued for its role as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The dihydrochloride form enhances solubility and stability, facilitating handling and reaction efficiency. Its reactive chloro group allows for further functionalization, making it useful in cross-coupling reactions and nucleophilic substitutions. The compound’s rigid fused-ring structure contributes to its utility in designing bioactive molecules. High purity and well-defined chemical properties ensure reproducibility in research and industrial applications.
2-Chloro-pyrido2,3-bpyrazine Dihydrochloride structure
1187931-12-9 structure
Product Name:2-Chloro-pyrido2,3-bpyrazine Dihydrochloride
CAS No:1187931-12-9
MF:C7H6Cl3N3
MW:238.501637935638
MDL:MFCD11506229
CID:4778077
Update Time:2026-02-27

2-Chloro-pyrido2,3-bpyrazine Dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride
    • 2-chloropyrido[2,3-b]pyrazine dihydrochloride
    • NE62897
    • SB31402
    • 2-Chloro-pyrido2,3-bpyrazine dihydrochloride
    • 2-Chloro-pyrido2,3-bpyrazine Dihydrochloride
    • MDL: MFCD11506229
    • Inchi: 1S/C7H4ClN3.2ClH/c8-6-4-10-7-5(11-6)2-1-3-9-7;;/h1-4H;2*1H
    • InChI Key: WAFWGVOTWBMAPR-UHFFFAOYSA-N
    • SMILES: ClC1=CN=C2C(C=CC=N2)=N1.Cl.Cl

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 0
  • Complexity: 142
  • Topological Polar Surface Area: 38.7

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Additional information on 2-Chloro-pyrido2,3-bpyrazine Dihydrochloride

Recent Advances in the Study of 2-Chloro-pyrido[2,3-b]pyrazine Dihydrochloride (CAS: 1187931-12-9)

2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride (CAS: 1187931-12-9) is a heterocyclic compound that has garnered significant attention in the field of chemical biology and medicinal chemistry due to its potential applications in drug discovery and development. Recent studies have focused on its role as a key intermediate in the synthesis of novel therapeutic agents, particularly in the areas of oncology and infectious diseases. This research brief aims to summarize the latest findings related to this compound, highlighting its chemical properties, biological activities, and potential clinical applications.

One of the most notable advancements in the study of 2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride is its incorporation into the design of kinase inhibitors. Kinases play a critical role in cellular signaling pathways, and their dysregulation is often associated with cancer and other diseases. Researchers have demonstrated that derivatives of this compound exhibit potent inhibitory activity against specific kinases, such as EGFR and BRAF, which are frequently mutated in various cancers. These findings suggest that 2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride could serve as a valuable scaffold for the development of targeted cancer therapies.

In addition to its applications in oncology, recent studies have explored the antimicrobial properties of 2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride. Preliminary in vitro assays have shown that this compound and its derivatives exhibit activity against a range of bacterial and fungal pathogens, including methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans. These results highlight the potential of this compound as a starting point for the development of new antimicrobial agents, particularly in light of the growing threat of antibiotic resistance.

The synthesis and optimization of 2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride derivatives have also been a focus of recent research. Advances in synthetic chemistry have enabled the efficient production of diverse analogs, allowing for structure-activity relationship (SAR) studies. These studies have provided valuable insights into the molecular features that contribute to the compound's biological activity, paving the way for the design of more potent and selective drug candidates.

Despite these promising developments, challenges remain in the translation of 2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride-based compounds into clinical applications. Issues such as bioavailability, toxicity, and pharmacokinetic properties need to be addressed through further preclinical studies. Nonetheless, the compound's versatility and demonstrated biological activities make it a compelling subject for ongoing research in the chemical biology and pharmaceutical sciences.

In conclusion, 2-Chloro-pyrido[2,3-b]pyrazine dihydrochloride (CAS: 1187931-12-9) represents a promising scaffold for the development of novel therapeutic agents. Recent studies have underscored its potential in oncology and antimicrobial therapy, while advances in synthetic chemistry have facilitated the exploration of its SAR. Future research should focus on addressing the remaining challenges to unlock the full therapeutic potential of this compound.

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