Cas no 1172715-34-2 (2-(1H-Pyrazol-1-yl)propanamide)
2-(1H-Pyrazol-1-yl)propanamide Chemical and Physical Properties
Names and Identifiers
-
- 2-(1H-pyrazol-1-yl)propanamide
- 2-pyrazolylpropanamide
- 2-(pyrazol-1-yl)propanamide
- SBB026041
- BBL016297
- STK352971
- 1H-pyrazole-1-acetamide, alpha-methyl-
- ST45134767
- 2-(1H-Pyrazol-1-yl)propanamide
-
- MDL: MFCD09859264
- Inchi: 1S/C6H9N3O/c1-5(6(7)10)9-4-2-3-8-9/h2-5H,1H3,(H2,7,10)
- InChI Key: CVZRDDTXGDTKOJ-UHFFFAOYSA-N
- SMILES: O=C(C(C)N1C=CC=N1)N
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 10
- Rotatable Bond Count: 2
- Complexity: 137
- Topological Polar Surface Area: 60.9
2-(1H-Pyrazol-1-yl)propanamide Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- HazardClass:IRRITANT
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
2-(1H-Pyrazol-1-yl)propanamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B530065-10mg |
2-(1H-Pyrazol-1-yl)propanamide |
1172715-34-2 | 10mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B530065-50mg |
2-(1H-Pyrazol-1-yl)propanamide |
1172715-34-2 | 50mg |
$ 115.00 | 2022-06-07 | ||
| TRC | B530065-100mg |
2-(1H-Pyrazol-1-yl)propanamide |
1172715-34-2 | 100mg |
$ 160.00 | 2022-06-07 | ||
| abcr | AB379782-250 mg |
2-(1H-Pyrazol-1-yl)propanamide |
1172715-34-2 | 250MG |
€198.50 | 2022-03-02 | ||
| abcr | AB379782-500 mg |
2-(1H-Pyrazol-1-yl)propanamide |
1172715-34-2 | 500MG |
€264.80 | 2022-03-02 | ||
| abcr | AB379782-1 g |
2-(1H-Pyrazol-1-yl)propanamide; . |
1172715-34-2 | 1g |
€462.00 | 2022-08-31 | ||
| abcr | AB379782-5 g |
2-(1H-Pyrazol-1-yl)propanamide; . |
1172715-34-2 | 5g |
€1,242.00 | 2022-08-31 | ||
| Chemenu | CM487320-1g |
2-(1H-Pyrazol-1-yl)propanamide |
1172715-34-2 | 97% | 1g |
$400 | 2022-06-14 | |
| abcr | AB379782-1g |
2-(1H-Pyrazol-1-yl)propanamide; . |
1172715-34-2 | 1g |
€477.00 | 2025-04-22 | ||
| abcr | AB379782-5g |
2-(1H-Pyrazol-1-yl)propanamide; . |
1172715-34-2 | 5g |
€1277.00 | 2025-04-22 |
2-(1H-Pyrazol-1-yl)propanamide Related Literature
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1. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
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Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
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Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
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Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471
Additional information on 2-(1H-Pyrazol-1-yl)propanamide
2-(1H-Pyrazol-1-yl)propanamide: A Versatile Chemical Compound with Emerging Applications
2-(1H-Pyrazol-1-yl)propanamide (CAS No. 1172715-34-2) is an intriguing organic compound that has garnered significant attention in recent years due to its unique structural features and potential applications in various scientific fields. This heterocyclic amide derivative combines the pyrazole moiety with a propanamide group, creating a molecular architecture that offers interesting chemical properties and biological activities.
The compound's molecular formula is C6H9N3O, with a molecular weight of 139.16 g/mol. Its structure features a 1H-pyrazole ring attached to the second carbon of a three-carbon amide chain, making it a valuable scaffold in medicinal chemistry and materials science. The presence of both hydrogen bond donor (amide NH) and acceptor (pyrazole N and amide carbonyl) groups contributes to its versatile interaction capabilities.
Recent studies have highlighted the potential of 2-(1H-Pyrazol-1-yl)propanamide derivatives in pharmaceutical research, particularly in the development of novel therapeutic agents. The pyrazole-propanamide hybrid structure has shown promise in modulating various biological targets, sparking interest among researchers investigating new treatment approaches for common health conditions.
In synthetic chemistry, 2-(1H-Pyrazol-1-yl)propanamide serves as a valuable building block for creating more complex molecular architectures. Its reactivity patterns allow for diverse chemical modifications at multiple sites, enabling the synthesis of libraries of compounds for structure-activity relationship studies. This characteristic makes it particularly valuable in drug discovery programs and materials science applications.
The compound's physicochemical properties have been the subject of several investigations. It typically appears as a white to off-white crystalline powder with good solubility in common organic solvents such as dimethyl sulfoxide (DMSO), methanol, and dimethylformamide (DMF). These solubility characteristics make it convenient for various experimental applications in both academic and industrial settings.
One of the most searched questions regarding 2-(1H-Pyrazol-1-yl)propanamide relates to its potential biological activities. While comprehensive pharmacological data is still emerging, preliminary studies suggest that derivatives of this compound may exhibit interesting biological properties, including potential modulation of enzymatic activity and receptor interactions. Researchers are particularly interested in its possible applications in addressing modern health challenges.
The synthesis of 2-(1H-Pyrazol-1-yl)propanamide typically involves the reaction of 1H-pyrazole with appropriate propanamide derivatives under controlled conditions. Modern synthetic approaches often employ catalytic methods and green chemistry principles to improve yield and reduce environmental impact, reflecting current trends in sustainable chemical production.
In material science applications, the pyrazole-propanamide hybrid structure has shown potential in the development of specialty materials. Its ability to form hydrogen-bonded networks and participate in various molecular interactions makes it interesting for designing functional materials with specific properties. This aligns well with current research trends in smart materials and nanotechnology.
Quality control of 2-(1H-Pyrazol-1-yl)propanamide typically involves analytical techniques such as high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR) spectroscopy, and mass spectrometry. These methods ensure the compound meets the required purity standards for research and potential applications, addressing another common query from researchers and procurement specialists.
The stability profile of 2-(1H-Pyrazol-1-yl)propanamide has been investigated under various conditions. Proper storage recommendations include keeping the compound in a cool, dry environment, protected from light and moisture. These storage conditions help maintain its chemical integrity over extended periods, which is crucial for research reproducibility and industrial applications.
Recent patent literature reveals growing interest in 2-(1H-Pyrazol-1-yl)propanamide-based compounds, particularly in pharmaceutical and agrochemical applications. Several patent filings describe derivatives of this compound with potential utility in addressing current challenges in human health and agricultural productivity, reflecting the compound's versatility and commercial potential.
From a safety perspective, standard laboratory precautions are recommended when handling 2-(1H-Pyrazol-1-yl)propanamide. While not classified as highly hazardous, proper personal protective equipment including gloves and safety glasses should be used, and operations should be conducted in well-ventilated areas. These precautions align with modern laboratory safety protocols and best practices.
The commercial availability of 2-(1H-Pyrazol-1-yl)propanamide has increased in recent years, with several specialty chemical suppliers offering the compound in various quantities. This improved accessibility has facilitated research into its potential applications and enabled more extensive structure-activity relationship studies by academic and industrial researchers worldwide.
Looking to the future, 2-(1H-Pyrazol-1-yl)propanamide and its derivatives represent an area of active investigation with promising prospects. As research continues to uncover new aspects of its chemistry and potential applications, this compound is likely to maintain its position as an interesting subject in scientific literature and a valuable tool in chemical research and development.
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