Cas no 17325-39-2 (2,6-Dimethoxypyridin-4-amine)
2,6-Dimethoxypyridin-4-amine Chemical and Physical Properties
Names and Identifiers
-
- 2,6-Dimethoxypyridin-4-amine
- 2,6-Dimethoxy-pyridin-4-ylamine
- 2,6-Dimethoxy-4-amino-pyridin
- 2,6-Dimethoxy-4-pyridinamine
- 2,6-dimethoxypyridine-4-amine
- 4-Amino-2,6-dimethoxypyridin
- 4-amino-2,6-dimethoxypyridine
- CTK8E3566
- QC-2131
- RL02218
- RW3649
- SureCN4716253
- 2,6-Dimethoxy-4-aminopyridin
- AJSGJCSWZUHDJB-UHFFFAOYSA-N
- 8938AA
- FCH1192749
- SY028009
- AK123397
- AX8247575
- AB0047946
- ST24038855
- A811499
- J-5
- DTXSID00623511
- SB53319
- SCHEMBL4716253
- CS-0036587
- F19757
- DS-2867
- AKOS016011864
- J-507498
- MFCD19688654
- FT-0737186
- 17325-39-2
- DA-09312
-
- MDL: MFCD19688654
- Inchi: 1S/C7H10N2O2/c1-10-6-3-5(8)4-7(9-6)11-2/h3-4H,1-2H3,(H2,8,9)
- InChI Key: AJSGJCSWZUHDJB-UHFFFAOYSA-N
- SMILES: O(C)C1C=C(C=C(N=1)OC)N
Computed Properties
- Exact Mass: 154.0743
- Monoisotopic Mass: 154.074227566g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 109
- 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
- Topological Polar Surface Area: 57.4
- XLogP3: 0.8
Experimental Properties
- Density: 1.159±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 82-83 oC (benzene ligroine )
- Solubility: Slightly soluble (7.4 g/l) (25 o C),
- PSA: 57.37
2,6-Dimethoxypyridin-4-amine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Matrix Scientific | 126099-1g |
2,6-Dimethoxypyridin-4-amine, >95% |
17325-39-2 | >95% | 1g |
$756.00 | 2023-09-07 | |
| ChemScence | CS-0036587-100mg |
2,6-Dimethoxypyridin-4-amine |
17325-39-2 | ≥97.0% | 100mg |
$132.0 | 2022-04-27 | |
| ChemScence | CS-0036587-250mg |
2,6-Dimethoxypyridin-4-amine |
17325-39-2 | ≥97.0% | 250mg |
$225.0 | 2022-04-27 | |
| ChemScence | CS-0036587-1g |
2,6-Dimethoxypyridin-4-amine |
17325-39-2 | ≥97.0% | 1g |
$495.0 | 2022-04-27 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | Y02735-1g |
4-Amino-2,6-dimethoxypyridine |
17325-39-2 | 95% | 1g |
¥6309.0 | 2023-09-05 | |
| Chemenu | CM131711-1g |
2,6-dimethoxypyridin-4-amine |
17325-39-2 | 97% | 1g |
$310 | 2021-08-05 | |
| Apollo Scientific | OR470868-1g |
4-Amino-2,6-dimethoxypyridine |
17325-39-2 | 1g |
£693.00 | 2023-09-01 | ||
| eNovation Chemicals LLC | Y0979404-1g |
2,6-dimethoxypyridin-4-amine |
17325-39-2 | 95% | 1g |
$475 | 2023-05-16 | |
| eNovation Chemicals LLC | D686118-0.25g |
4-Amino-2,6-dimethoxypyridine |
17325-39-2 | 97% | 0.25g |
$175 | 2024-07-20 | |
| eNovation Chemicals LLC | D686118-1g |
4-Amino-2,6-dimethoxypyridine |
17325-39-2 | 97% | 1g |
$385 | 2024-07-20 |
2,6-Dimethoxypyridin-4-amine Suppliers
2,6-Dimethoxypyridin-4-amine Related Literature
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
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Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
Additional information on 2,6-Dimethoxypyridin-4-amine
2,6-Dimethoxypyridin-4-amine (CAS No. 17325-39-2)
2,6-Dimethoxypyridin-4-amine is a versatile organic compound with the CAS registry number 17325-39-2. This compound belongs to the class of pyridine derivatives and has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields. The molecule consists of a pyridine ring substituted with methoxy groups at the 2 and 6 positions and an amino group at the 4 position. This substitution pattern imparts 2,6-Dimethoxypyridin-4-amine with distinct electronic and steric properties, making it a valuable compound in both academic research and industrial applications.
Recent studies have highlighted the role of 2,6-Dimethoxypyridin-4-amine in medicinal chemistry. Researchers have explored its potential as a precursor for synthesizing bioactive molecules, particularly in the development of novel antibiotics and anticancer agents. The methoxy groups at positions 2 and 6 contribute to the compound's lipophilicity, enhancing its ability to cross cellular membranes. This property is crucial for designing drugs that can effectively target intracellular pathogens or cancer cells.
In addition to its role in drug discovery, 2,6-Dimethoxypyridin-4-amine has been utilized as an intermediate in the synthesis of advanced materials. For instance, it has been employed in the preparation of conductive polymers and metalloorganic frameworks (MOFs). The amino group at position 4 facilitates coordination with metal ions, enabling the formation of stable metal-ligand complexes. These complexes exhibit promising catalytic activity in various organic transformations, making them valuable tools in green chemistry.
The synthesis of 2,6-Dimethoxypyridin-4-amine typically involves multi-step processes that combine substitution and condensation reactions. One common approach involves the nucleophilic substitution of a pyridine derivative with methoxy groups followed by amination at the 4 position. Recent advancements in catalytic methods have improved the efficiency and selectivity of these reactions, leading to higher yields of 17325-39-2.
From an environmental perspective, researchers have investigated the biodegradation pathways of 2,6-Dimethoxypyridin-4-amine to assess its ecological impact. Studies indicate that under aerobic conditions, the compound undergoes microbial degradation through oxidative cleavage of the pyridine ring. This information is critical for ensuring sustainable practices in industries that utilize this compound.
In conclusion, 2,6-Dimethoxypyridin-4-amine (CAS No. 17325-39-2) stands out as a multifaceted compound with diverse applications across chemistry and materials science. Its unique structure enables it to serve as both a building block for advanced materials and a precursor for bioactive molecules. As research continues to uncover new properties and uses for this compound, its significance in both academic and industrial settings is expected to grow further.
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