Cas no 1296308-08-1 (1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol)
1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol Chemical and Physical Properties
Names and Identifiers
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- 1-(4-amino-1H-pyrazol-1-yl)propan-2-ol
- 1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol
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- Inchi: 1S/C6H11N3O/c1-5(10)3-9-4-6(7)2-8-9/h2,4-5,10H,3,7H2,1H3
- InChI Key: RSQSEMKMQIULTM-UHFFFAOYSA-N
- SMILES: OC(C)CN1C=C(C=N1)N
Computed Properties
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 10
- Rotatable Bond Count: 2
- Complexity: 109
- Topological Polar Surface Area: 64.099
1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-783422-0.05g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 0.05g |
$256.0 | 2025-02-22 | |
| Enamine | EN300-783422-0.1g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 0.1g |
$383.0 | 2025-02-22 | |
| Enamine | EN300-783422-0.25g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 0.25g |
$546.0 | 2025-02-22 | |
| Enamine | EN300-783422-0.5g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 0.5g |
$858.0 | 2025-02-22 | |
| Enamine | EN300-783422-1.0g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 1.0g |
$1100.0 | 2025-02-22 | |
| Enamine | EN300-783422-2.5g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 2.5g |
$2155.0 | 2025-02-22 | |
| Enamine | EN300-783422-5.0g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 5.0g |
$3189.0 | 2025-02-22 | |
| Enamine | EN300-783422-10.0g |
1-(4-amino-1H-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 95.0% | 10.0g |
$4729.0 | 2025-02-22 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1332053-50mg |
1-(4-Amino-1h-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 98% | 50mg |
¥6451.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1332053-100mg |
1-(4-Amino-1h-pyrazol-1-yl)propan-2-ol |
1296308-08-1 | 98% | 100mg |
¥8268.00 | 2024-08-09 |
1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol Related Literature
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Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
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Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
Additional information on 1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol
Introduction to 1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol (CAS No. 1296308-08-1)
1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol (CAS No. 1296308-08-1) is a versatile compound with significant potential in various fields of chemistry and materials science. This compound, characterized by its unique structure, has garnered attention due to its ability to participate in diverse chemical reactions and its role in the synthesis of advanced materials. The molecule consists of a pyrazole ring, an amino group, and a secondary alcohol functional group, making it a valuable building block in organic synthesis.
The pyrazole ring is a five-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. In 1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol, the amino group is attached at position 4 of the pyrazole ring, while the propanol group is attached at position 1. This arrangement imparts the molecule with unique electronic properties and reactivity, which are exploited in various chemical transformations.
Recent studies have highlighted the role of pyrazole derivatives in the development of novel pharmaceuticals, agrochemicals, and advanced materials. For instance, researchers have explored the use of pyrazole-containing compounds in the synthesis of biodegradable polymers, which hold promise for sustainable packaging solutions. The presence of the amino group in 1-(4-Amino-1H-pyrazol-1-yl)propan-2-ol allows for further functionalization, enabling the creation of tailor-made materials with specific properties.
The synthesis of CAS No. 1296308-08-1 involves a multi-step process that typically begins with the preparation of pyrazole derivatives. One common approach involves the condensation of an aldehyde or ketone with ammonia or ammonium salts, followed by cyclization to form the pyrazole ring. Subsequent modifications introduce the amino and propanol groups, resulting in the final compound.
In terms of applications, pyrazole derivatives like CAS No. 1296308-08-1 are widely used as intermediates in organic synthesis. They serve as precursors for the preparation of pharmaceutical agents, agrochemicals, and specialty chemicals. For example, recent research has demonstrated their utility in the development of antiviral drugs targeting emerging pathogens such as coronaviruses.
Moreover, pyrazole-containing compounds have found applications in catalysis and materials science. Their ability to coordinate with metal ions makes them valuable ligands in homogeneous catalysis for processes such as hydrogenation and oxidation reactions. Additionally, they are being explored for their potential in creating stimuli-responsive materials that can adapt to environmental changes such as temperature or pH levels.
The physical properties of CAS No. 1296308-08-1 include a melting point of approximately 75°C and a boiling point around 350°C under standard conditions. The compound is soluble in common organic solvents such as ethanol and dichloromethane but exhibits limited solubility in water due to its hydrophobic nature.
From an environmental standpoint, studies have shown that pyrazole derivatives can undergo biodegradation under aerobic conditions, making them less persistent in natural environments compared to other synthetic compounds. However, their impact on aquatic ecosystems remains an area of active research to ensure their safe use and disposal.
In conclusion, CAS No. 1296308-08 - - (Product Name: - ) stands out as a valuable compound with diverse applications across multiple disciplines. Its unique structure enables it to serve as a versatile building block for synthesizing advanced materials and pharmaceuticals while maintaining compatibility with modern green chemistry principles.
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