Cas no 68336-81-2 (5-Bromo-1,6-naphthyridine)
5-Bromo-1,6-naphthyridine Chemical and Physical Properties
Names and Identifiers
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- 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 Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| eNovation Chemicals LLC | Y1267197-1g |
5-Bromo-1,6-naphthyridine |
68336-81-2 | 95% | 1g |
$655 | 2024-06-07 | |
| eNovation Chemicals LLC | Y1267197-5g |
5-Bromo-1,6-naphthyridine |
68336-81-2 | 95% | 5g |
$2625 | 2024-06-07 | |
| Enamine | EN300-295368-0.05g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 0.05g |
$174.0 | 2023-09-06 | |
| Enamine | EN300-295368-0.1g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 0.1g |
$257.0 | 2023-09-06 | |
| Enamine | EN300-295368-0.25g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 0.25g |
$367.0 | 2023-09-06 | |
| Enamine | EN300-295368-0.5g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 0.5g |
$579.0 | 2023-09-06 | |
| Enamine | EN300-295368-1.0g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 1g |
$743.0 | 2023-06-04 | |
| Enamine | EN300-295368-2.5g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 2.5g |
$1454.0 | 2023-09-06 | |
| Enamine | EN300-295368-5.0g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 5g |
$2152.0 | 2023-06-04 | |
| Enamine | EN300-295368-10.0g |
5-bromo-1,6-naphthyridine |
68336-81-2 | 95% | 10g |
$3191.0 | 2023-06-04 |
5-Bromo-1,6-naphthyridine Suppliers
5-Bromo-1,6-naphthyridine Related Literature
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Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431
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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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.
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