Cas no 36057-54-2 (2-Pyridinecarboxamide, 3-bromo-)

2-Pyridinecarboxamide, 3-bromo-, is a brominated pyridine derivative with significant utility in organic synthesis and pharmaceutical research. The presence of both a carboxamide group and a bromine substituent at the 3-position enhances its reactivity, making it a versatile intermediate for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Its structural features also facilitate further functionalization, enabling the synthesis of complex heterocyclic compounds. The compound's well-defined reactivity and stability under standard conditions make it a reliable choice for medicinal chemistry applications, particularly in the development of bioactive molecules. High purity and consistent quality ensure reproducibility in research and industrial processes.
2-Pyridinecarboxamide, 3-bromo- structure
36057-54-2 structure
Product Name:2-Pyridinecarboxamide, 3-bromo-
CAS No:36057-54-2
MF:C6H5BrN2O
MW:201.020700216293
MDL:MFCD11043941
CID:1473031
PubChem ID:21529157
Update Time:2025-10-11

2-Pyridinecarboxamide, 3-bromo- Chemical and Physical Properties

Names and Identifiers

    • 2-Pyridinecarboxamide, 3-bromo-
    • 2-Pyridinecarboxamide,3-bromo
    • SCHEMBL518833
    • 36057-54-2
    • BS-51164
    • MFCD11043941
    • D83286
    • 3-bromopicolinamide
    • ZIWGQZWSTOEFEP-UHFFFAOYSA-N
    • SB77457
    • 3-BROMO-PYRIDINE-2-CARBOXYLIC ACID AMIDE
    • AKOS026737597
    • 3-Bromopyridine-2-carboxamide
    • CS-0149986
    • MDL: MFCD11043941
    • Inchi: 1S/C6H5BrN2O/c7-4-2-1-3-9-5(4)6(8)10/h1-3H,(H2,8,10)
    • InChI Key: ZIWGQZWSTOEFEP-UHFFFAOYSA-N
    • SMILES: BrC1=CC=CN=C1C(N)=O

Computed Properties

  • Exact Mass: 199.95855
  • Monoisotopic Mass: 199.95853g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 140
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.1
  • Topological Polar Surface Area: 56?2

Experimental Properties

  • PSA: 55.98

2-Pyridinecarboxamide, 3-bromo- Pricemore >>

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Additional information on 2-Pyridinecarboxamide, 3-bromo-

Professional Introduction of 3-Bromo-2-Pyridinecarboxamide (CAS No. 36057-54-2)

The compound 3-bromo-2-pyridinecarboxamide, also known by its CAS number 36057-54-2, is a versatile organic molecule that has garnered significant attention in the fields of medicinal chemistry and materials science. This compound belongs to the class of pyridine derivatives, characterized by the presence of a bromine substituent at position 3 and an amide group at position 2 on the aromatic ring. The structure of this compound makes it a valuable tool for various applications, including drug discovery, catalysis, and molecular recognition.

In recent years, there has been a growing interest in pyridine-based compounds due to their unique electronic properties and ability to participate in diverse chemical reactions. The bromine atom at position 3 introduces electron-withdrawing effects, which can influence the reactivity of the molecule and its interactions with other components. This makes 3-bromo-2-pyridinecarboxamide particularly useful in transition metal catalysis, where such directing effects are crucial for controlling reaction pathways.

The amide group at position 2 adds another layer of functionality to this compound, enabling it to act as a potential ligand in metal coordination complexes. Amides are known for their ability to form stable bonds with metal centers, making them valuable in the development of catalysts for various transformations, including cross-coupling reactions and hydrogenation processes. The combination of these functional groups positions 3-bromo-2-pyridinecarboxamide as a promising candidate for heterocyclic chemistry and sustainable chemical synthesis.

Recent studies have highlighted the potential of this compound in biomedical applications. For instance, its pyridine ring can serve as a scaffold for attaching bioactive groups, such as antibiotics or antiviral agents. The bromine substituent may also play a role in modulating pharmacokinetics, thereby enhancing the efficacy of potential therapeutic agents derived from this structure.

Moreover, 3-bromo-2-pyridinecarboxamide has been explored in the context of nanochemistry. The molecule's ability to form coordination bonds with metal nanoparticles makes it a candidate for use in stabilizing and functionalizing such materials. This could open up new avenues in fields like catalysis, sensing, and energy storage.

Despite its potential, there remain challenges in fully harnessing the capabilities of this compound. For instance, optimizing its synthesis to achieve higher yields while maintaining purity remains a critical area of research. Additionally, understanding its environmental impact and ensuring its safe handling are essential considerations for large-scale applications.

In conclusion, 3-bromo-2-pyridinecarboxamide (CAS No. 36057-54-2) stands out as a multifaceted compound with wide-ranging applications in chemistry and beyond. Its unique structure, combining bromine and amide functionalities on a pyridine ring, makes it a valuable asset for researchers seeking to advance medicinal chemistry, catalysis, and nanochemistry. As scientific research continues to uncover new possibilities, this compound is poised to play an increasingly important role in addressing complex chemical and biomedical challenges.

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