Cas no 36057-54-2 (2-Pyridinecarboxamide, 3-bromo-)
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 >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029208224-5g |
3-Bromopicolinamide |
36057-54-2 | 97% | 5g |
$520.56 | 2023-09-02 | |
| Alichem | A029208224-10g |
3-Bromopicolinamide |
36057-54-2 | 97% | 10g |
$585.52 | 2023-09-02 | |
| Alichem | A029208224-25g |
3-Bromopicolinamide |
36057-54-2 | 97% | 25g |
$1025.10 | 2023-09-02 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-HY608-50mg |
2-Pyridinecarboxamide, 3-bromo- |
36057-54-2 | 97% | 50mg |
89.0CNY | 2021-07-15 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-HY608-200mg |
2-Pyridinecarboxamide, 3-bromo- |
36057-54-2 | 97% | 200mg |
182.0CNY | 2021-07-15 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-HY608-1g |
2-Pyridinecarboxamide, 3-bromo- |
36057-54-2 | 97% | 1g |
522.0CNY | 2021-07-15 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-HY608-5g |
2-Pyridinecarboxamide, 3-bromo- |
36057-54-2 | 97% | 5g |
1828.0CNY | 2021-07-15 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1220626-250mg |
3-Bromopicolinamide |
36057-54-2 | 98% | 250mg |
¥205.00 | 2024-05-16 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1220626-25g |
3-Bromopicolinamide |
36057-54-2 | 98% | 25g |
¥3896.00 | 2024-05-16 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | B45725-1g |
3-Bromopicolinamide |
36057-54-2 | 97% | 1g |
¥304.0 | 2024-07-16 |
2-Pyridinecarboxamide, 3-bromo- Related Literature
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
-
Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
-
Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
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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