Cas no 1595921-61-1 (1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine)
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine Chemical and Physical Properties
Names and Identifiers
-
- 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine
- EN300-1108234
- 1595921-61-1
- SCHEMBL18494112
-
- Inchi: 1S/C8H15N3O/c1-7(3-4-12-2)11-6-8(9)5-10-11/h5-7H,3-4,9H2,1-2H3
- InChI Key: QRNHBUQDUOMIPE-UHFFFAOYSA-N
- SMILES: O(C)CCC(C)N1C=C(C=N1)N
Computed Properties
- Exact Mass: 169.121512110g/mol
- Monoisotopic Mass: 169.121512110g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 4
- Complexity: 132
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.1
- Topological Polar Surface Area: 53.1?2
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1108234-0.05g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 95% | 0.05g |
$647.0 | 2023-10-27 | |
| Enamine | EN300-1108234-0.1g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 95% | 0.1g |
$678.0 | 2023-10-27 | |
| Enamine | EN300-1108234-0.25g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 95% | 0.25g |
$708.0 | 2023-10-27 | |
| Enamine | EN300-1108234-0.5g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 95% | 0.5g |
$739.0 | 2023-10-27 | |
| Enamine | EN300-1108234-1.0g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 1g |
$1299.0 | 2023-05-24 | ||
| Enamine | EN300-1108234-2.5g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 95% | 2.5g |
$1509.0 | 2023-10-27 | |
| Enamine | EN300-1108234-5.0g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 5g |
$3770.0 | 2023-05-24 | ||
| Enamine | EN300-1108234-10.0g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 10g |
$5590.0 | 2023-05-24 | ||
| Enamine | EN300-1108234-1g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 95% | 1g |
$770.0 | 2023-10-27 | |
| Enamine | EN300-1108234-5g |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine |
1595921-61-1 | 95% | 5g |
$2235.0 | 2023-10-27 |
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine Related Literature
-
Jason Wan Lab Chip, 2020,20, 4528-4538
-
Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
-
Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
-
Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
-
Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
Additional information on 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine
Comprehensive Overview of 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine (CAS No. 1595921-61-1)
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine (CAS No. 1595921-61-1) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique pyrazole core and methoxybutyl side chain, is a promising intermediate for the synthesis of bioactive molecules. Researchers are increasingly exploring its potential applications due to its structural versatility and functional group compatibility. The amine moiety at the 4-position of the pyrazole ring enhances its reactivity, making it a valuable building block in drug discovery and material science.
In recent years, the demand for 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine has surged, driven by its relevance in developing novel kinase inhibitors and antimicrobial agents. The compound's CAS No. 1595921-61-1 is frequently searched in academic and industrial databases, reflecting its growing importance. Its synthesis typically involves multi-step organic reactions, including N-alkylation and amination, which are well-documented in peer-reviewed journals. The compound's stability under physiological conditions further underscores its potential for biomedical applications.
One of the most discussed topics in the context of 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine is its role in targeted drug delivery systems. The methoxybutyl group improves solubility, a critical factor for oral bioavailability. This aligns with current trends in personalized medicine, where researchers seek compounds with optimized pharmacokinetic profiles. Additionally, the pyrazole scaffold is known for its anti-inflammatory and antioxidant properties, making this compound a candidate for treating chronic diseases.
From an industrial perspective, CAS No. 1595921-61-1 is often associated with green chemistry initiatives. Manufacturers are exploring eco-friendly synthesis routes to minimize waste and reduce energy consumption. This resonates with the global push for sustainable chemical production, a topic frequently queried in search engines. The compound's compatibility with catalytic processes further enhances its appeal for large-scale applications.
Another area of interest is the compound's potential in crop protection. The amine functionality allows for derivatization into agrochemicals with enhanced efficacy against pests and pathogens. Given the rising focus on food security, this application is highly relevant. Researchers are also investigating its use in biodegradable polymers, leveraging its structural features to create environmentally friendly materials.
In summary, 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine (CAS No. 1595921-61-1) is a multifaceted compound with broad applicability. Its pyrazole-amine architecture, combined with the methoxybutyl side chain, offers unparalleled opportunities in drug development, material science, and agriculture. As research progresses, this compound is poised to play a pivotal role in addressing some of the most pressing challenges in modern science.
1595921-61-1 (1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine) Related Products
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
- 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
- 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)