Cas no 1589503-98-9 (6-Methoxypyridazin-3-amine hydrochloride)
6-Methoxypyridazin-3-amine hydrochloride Chemical and Physical Properties
Names and Identifiers
-
- 6-methoxypyridazin-3-amine hydrochloride
- SB10579
- 3-amino-6-methoxypyridazine hydrochloride
- 3-Pyridazinamine, 6-methoxy-, hydrochloride (1:1)
- SMQXTAFGVWBZDG-UHFFFAOYSA-N
- CS-0093822
- AKOS037651239
- 3-Amino-6-Methoxypyridazine HCl
- D75466
- 6-methoxypyridazin-3-aminehydrochloride
- LQB4255WMK
- CS-16226
- 1589503-98-9
- SCHEMBL16964217
- DB-118737
- 6-methoxypyridazin-3-amine;hydrochloride
- 6-Methoxypyridazin-3-amine hydrochloride
-
- Inchi: 1S/C5H7N3O.ClH/c1-9-5-3-2-4(6)7-8-5;/h2-3H,1H3,(H2,6,7);1H
- InChI Key: SMQXTAFGVWBZDG-UHFFFAOYSA-N
- SMILES: Cl.O(C)C1=CC=C(N)N=N1
Computed Properties
- Exact Mass: 161.0355896g/mol
- Monoisotopic Mass: 161.0355896g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 10
- Rotatable Bond Count: 1
- Complexity: 88.3
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 61
6-Methoxypyridazin-3-amine hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM327109-1000g |
6-methoxypyridazin-3-aminehydrochloride |
1589503-98-9 | 95%+ | 1000g |
$3600 | 2021-08-18 | |
| eNovation Chemicals LLC | Y1232808-5g |
3-Pyridazinamine, 6-methoxy-, hydrochloride (1:1) |
1589503-98-9 | 98% | 5g |
$200 | 2024-06-07 | |
| eNovation Chemicals LLC | Y1232808-10g |
3-Pyridazinamine, 6-methoxy-, hydrochloride (1:1) |
1589503-98-9 | 98% | 10g |
$315 | 2024-06-07 | |
| Chemenu | CM327109-1g |
6-methoxypyridazin-3-aminehydrochloride |
1589503-98-9 | 95%+ | 1g |
$58 | 2023-03-07 | |
| Chemenu | CM327109-5g |
6-methoxypyridazin-3-aminehydrochloride |
1589503-98-9 | 95%+ | 5g |
$177 | 2023-03-07 | |
| Chemenu | CM327109-10g |
6-methoxypyridazin-3-aminehydrochloride |
1589503-98-9 | 95%+ | 10g |
$300 | 2023-03-07 | |
| Chemenu | CM327109-25g |
6-methoxypyridazin-3-aminehydrochloride |
1589503-98-9 | 95%+ | 25g |
$600 | 2023-03-07 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PB03619-1-1G |
6-methoxypyridazin-3-amine hydrochloride |
1589503-98-9 | 95% | 1g |
¥ 290.00 | 2023-03-07 | |
| 1PlusChem | 1P001RI7-250mg |
3-Pyridazinamine, 6-methoxy-, hydrochloride (1:1) |
1589503-98-9 | 98% | 250mg |
$108.00 | 2024-06-20 | |
| 1PlusChem | 1P001RI7-1g |
3-Pyridazinamine, 6-methoxy-, hydrochloride (1:1) |
1589503-98-9 | 98% | 1g |
$129.00 | 2024-06-20 |
6-Methoxypyridazin-3-amine hydrochloride Suppliers
6-Methoxypyridazin-3-amine hydrochloride Related Literature
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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4. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
Additional information on 6-Methoxypyridazin-3-amine hydrochloride
6-Methoxypyridazin-3-amine Hydrochloride: A Comprehensive Overview
The compound 6-Methoxypyridazin-3-amine hydrochloride (CAS No. 1589503-98-9) is a fascinating molecule with significant potential in various fields of chemistry and pharmacology. This compound belongs to the class of pyridazine derivatives, which have been extensively studied due to their unique electronic properties and biological activities. The methoxy group at position 6 and the amino group at position 3 of the pyridazine ring contribute to its distinctive chemical behavior and reactivity.
Recent advancements in synthetic chemistry have enabled the precise synthesis of 6-Methoxypyridazin-3-amine hydrochloride, allowing researchers to explore its properties in greater depth. The hydrochloride salt form of this compound is particularly advantageous for pharmaceutical applications, as it enhances solubility and stability. Studies have shown that this compound exhibits antimicrobial activity, making it a promising candidate for the development of new antibiotics.
In addition to its antimicrobial properties, 6-Methoxypyridazin-3-amine hydrochloride has demonstrated potential in the field of cancer research. Preclinical studies suggest that this compound may inhibit the growth of certain cancer cell lines by targeting specific signaling pathways. These findings align with broader trends in oncology research, where pyridazine derivatives are increasingly being explored for their anticancer potential.
The synthesis of 6-Methoxypyridazin-3-amine hydrochloride involves a multi-step process that includes nucleophilic substitution and acid-base neutralization. Researchers have optimized these steps to achieve high yields and purity, ensuring that the compound is suitable for both laboratory studies and potential clinical applications. The use of advanced analytical techniques, such as NMR spectroscopy and mass spectrometry, has further validated the structural integrity of this compound.
One of the most exciting aspects of 6-Methoxypyridazin-3-amine hydrochloride is its versatility in chemical reactions. Its ability to act as both a nucleophile and an electrophile makes it a valuable building block in organic synthesis. For instance, it can be used to construct more complex molecules with diverse functional groups, opening up new avenues for drug discovery and material science.
Looking ahead, the continued exploration of 6-Methoxypyridazin-3-amine hydrochloride is expected to yield further insights into its therapeutic applications. Collaborative efforts between academic institutions and pharmaceutical companies are likely to accelerate the translation of this compound into clinical use. As research progresses, it is anticipated that this molecule will play a pivotal role in advancing our understanding of pyridazine chemistry and its relevance to human health.
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