Cas no 68336-81-2 (5-Bromo-1,6-naphthyridine)

5-Bromo-1,6-naphthyridine is a halogenated heterocyclic compound featuring a naphthyridine core substituted with a bromine atom at the 5-position. This structure imparts reactivity suitable for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Its bromine substituent enhances versatility in further functionalization, while the 1,6-naphthyridine scaffold contributes to potential biological activity. The compound is typically characterized by high purity and stability, ensuring reliable performance in research and industrial applications. Its utility in constructing complex molecular architectures underscores its importance in medicinal chemistry and material science.
5-Bromo-1,6-naphthyridine structure
5-Bromo-1,6-naphthyridine structure
Product Name:5-Bromo-1,6-naphthyridine
CAS No:68336-81-2
MF:C8H5BrN2
MW:209.042700529099
MDL:MFCD00234383
CID:837975
PubChem ID:12460449
Update Time:2025-05-23

5-Bromo-1,6-naphthyridine Chemical and Physical Properties

Names and Identifiers

    • 5-Bromo-1,6-naphthyridine
    • FT-0750840
    • EN300-295368
    • SCHEMBL11509799
    • CS-0244830
    • DTXSID80499150
    • MFCD00234383
    • AKOS016002577
    • 68336-81-2
    • MB01013
    • MDL: MFCD00234383
    • Inchi: 1S/C8H5BrN2/c9-8-6-2-1-4-10-7(6)3-5-11-8/h1-5H
    • InChI Key: KOYAMUDOJYCKNF-UHFFFAOYSA-N
    • SMILES: BrC1C2=CC=CN=C2C=CN=1

Computed Properties

  • Exact Mass: 207.96361g/mol
  • Monoisotopic Mass: 207.96361g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 0
  • 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: 2.1
  • Topological Polar Surface Area: 25.8?2

5-Bromo-1,6-naphthyridine Security Information

  • Storage Condition:Sealed in dry,2-8°C(BD229215)

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5-Bromo-1,6-naphthyridine Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:68336-81-2)5-Bromo-1,6-naphthyridine
Order Number:A1228596
Stock Status:in Stock
Quantity:5g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 19:05
Price ($):3169

5-Bromo-1,6-naphthyridine Related Literature

Additional information on 5-Bromo-1,6-naphthyridine

5-Bromo-1,6-Naphthyridine: A Comprehensive Overview

5-Bromo-1,6-naphthyridine, also known by its CAS number 68336-81-2, is a heterocyclic aromatic compound with significant applications in various fields of chemistry. This compound belongs to the naphthyridine family, which is a fused bicyclic system consisting of a benzene ring and a pyridine ring. The bromine substituent at the 5-position introduces unique electronic and structural properties, making it a valuable compound in both academic research and industrial applications.

The synthesis of 5-Bromo-1,6-naphthyridine typically involves multi-step processes that include condensation reactions and bromination. Recent advancements in synthetic methodologies have focused on improving the efficiency and selectivity of these reactions. For instance, researchers have explored the use of microwave-assisted synthesis to accelerate the formation of naphthyridine derivatives, including 5-Bromo-1,6-naphthyridine. This approach not only reduces reaction time but also enhances the purity of the final product.

In terms of applications, 5-Bromo-1,6-naphthyridine has been extensively studied for its potential in pharmaceutical chemistry. The compound exhibits interesting pharmacological properties, particularly as a precursor for bioactive molecules. Recent studies have highlighted its role in the development of anti-inflammatory agents and anticancer drugs. For example, derivatives of 5-Bromo-1,6-naphthyridine have shown promising results in inhibiting key enzymes associated with inflammation and cancer cell proliferation.

The electronic properties of 5-Bromo-1,6-naphthyridine make it an attractive candidate for use in organic electronics. Its conjugated π-system facilitates efficient charge transport, which is crucial for applications such as organic light-emitting diodes (OLEDs) and field-effect transistors (FETs). Researchers have explored the integration of 5-Bromo-1,6-naphthyridine into polymer blends to enhance their electronic performance. These studies underscore the potential of this compound in advancing next-generation electronic materials.

In addition to its chemical applications, 5-Bromo-1,6-naphthyridine has gained attention in materials science due to its thermal stability and mechanical robustness. Recent investigations have focused on incorporating this compound into high-performance polymers for use in aerospace and automotive industries. The ability of 5-Bromo-1,6-naphthyridine to withstand extreme conditions without degradation makes it a valuable additive in polymer formulations.

The environmental impact of synthesizing and using 5-Bromo-1,6-naphthyridine has also been a topic of interest. Researchers have developed eco-friendly synthesis routes that minimize waste generation and reduce the use of hazardous solvents. These green chemistry approaches align with global efforts to promote sustainable practices in chemical manufacturing.

In conclusion, 5-Bromo-1,6-naphthyridine, with its unique chemical properties and diverse applications, remains a focal point in contemporary chemical research. From pharmaceuticals to electronics and materials science, this compound continues to demonstrate its versatility and importance across various disciplines. As research progresses, new insights into its potential uses are expected to emerge, further solidifying its role as a key compound in modern chemistry.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:68336-81-2)5-Bromo-1,6-naphthyridine
A1228596
Purity:99%
Quantity:5g
Price ($):3169
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