Cas no 1691973-43-9 ((1-ethenyl-1H-pyrazol-4-yl)methanamine)
(1-ethenyl-1H-pyrazol-4-yl)methanamine Chemical and Physical Properties
Names and Identifiers
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- (1-ethenyl-1H-pyrazol-4-yl)methanamine
- EN300-1867798
- 1691973-43-9
-
- Inchi: 1S/C6H9N3/c1-2-9-5-6(3-7)4-8-9/h2,4-5H,1,3,7H2
- InChI Key: MLUNEFGKCNQCAO-UHFFFAOYSA-N
- SMILES: N1(C=C)C=C(C=N1)CN
Computed Properties
- Exact Mass: 123.079647300g/mol
- Monoisotopic Mass: 123.079647300g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 9
- Rotatable Bond Count: 2
- Complexity: 103
- 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: -0.3
- Topological Polar Surface Area: 43.8?2
(1-ethenyl-1H-pyrazol-4-yl)methanamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1867798-0.05g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 0.05g |
$528.0 | 2023-09-18 | ||
| Enamine | EN300-1867798-0.1g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 0.1g |
$553.0 | 2023-09-18 | ||
| Enamine | EN300-1867798-0.25g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 0.25g |
$579.0 | 2023-09-18 | ||
| Enamine | EN300-1867798-0.5g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 0.5g |
$603.0 | 2023-09-18 | ||
| Enamine | EN300-1867798-1.0g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 1g |
$1343.0 | 2023-06-01 | ||
| Enamine | EN300-1867798-2.5g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 2.5g |
$1230.0 | 2023-09-18 | ||
| Enamine | EN300-1867798-5.0g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 5g |
$3894.0 | 2023-06-01 | ||
| Enamine | EN300-1867798-10.0g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 10g |
$5774.0 | 2023-06-01 | ||
| Enamine | EN300-1867798-1g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 1g |
$628.0 | 2023-09-18 | ||
| Enamine | EN300-1867798-5g |
(1-ethenyl-1H-pyrazol-4-yl)methanamine |
1691973-43-9 | 5g |
$1821.0 | 2023-09-18 |
(1-ethenyl-1H-pyrazol-4-yl)methanamine Related Literature
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
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Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Daniel Messmer,Stefan Salentinig,Jakob Heier Nanoscale, 2019,11, 6929-6938
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
Additional information on (1-ethenyl-1H-pyrazol-4-yl)methanamine
Introduction to 1-Ethenyl-1H-Pyrazol-4-Yl Methanamine (CAS No. 1691973-43-9)
The compound 1-Ethenyl-1H-Pyrazol-4-Yl Methanamine, identified by the CAS registry number 1691973-43-9, is a fascinating molecule with significant potential in various fields of chemistry and materials science. This compound belongs to the class of heterocyclic amines, specifically featuring a pyrazole ring substituted with an ethenyl group and a methanamine moiety. Its unique structure endows it with distinctive chemical properties, making it a subject of interest in both academic research and industrial applications.
Recent studies have highlighted the importance of pyrazole derivatives in drug discovery, particularly in the development of novel therapeutics targeting various diseases. The presence of the ethenyl group in this compound introduces additional reactivity, enabling it to participate in a wide range of chemical reactions. For instance, researchers have explored its potential as a building block for constructing more complex molecules with enhanced biological activity.
In terms of synthesis, the preparation of 1-Ethenyl-1H-Pyrazol-4-Yl Methanamine typically involves multi-step processes that combine traditional organic synthesis techniques with modern catalytic methods. One notable approach involves the reaction of pyrazole derivatives with alkenes under specific conditions to introduce the ethenyl group. This method has been optimized in recent years to improve yield and selectivity, reflecting advancements in synthetic chemistry.
The application of this compound extends beyond pharmaceuticals. In materials science, it has been investigated as a precursor for the synthesis of advanced materials, such as coordination polymers and metal-organic frameworks (MOFs). Its ability to coordinate with metal ions makes it a valuable component in constructing porous materials with applications in gas storage and catalysis.
From an environmental perspective, understanding the behavior of 1-Ethenyl-1H-Pyrazol-4-Yl Methanamine in different conditions is crucial for assessing its safety and sustainability. Recent toxicological studies have focused on its potential ecotoxicity and biodegradability, providing insights into its environmental impact. These findings are essential for guiding its responsible use in industrial processes.
In conclusion, the compound 1-Ethenyl-1H-Pyrazol-4-Yl Methanamine (CAS No. 1691973-43-9) represents a versatile molecule with diverse applications across multiple disciplines. Its unique chemical properties, coupled with ongoing research into its synthesis and applications, position it as a key player in advancing modern chemistry and materials science.
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