Cas no 28024-60-4 (2-amino-3-(1H-pyrazol-1-yl)propanoic acid)
2-amino-3-(1H-pyrazol-1-yl)propanoic acid Chemical and Physical Properties
Names and Identifiers
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- 2-Amino-3-(1-pyrazolyl)propanoic Acid
- (±)-alpha-amino-1H-pyrazole-1-propionic acid
- 1H-Pyrazole-1-propanoicacid, a-amino-
- 2-Amino-3-pyrazol-1-yl-propionic acid
- 3-(1H-Pyrazol-1-yl)alanine
- 2-amino-3-phosphonopropionate
- 2-Amino-3-phosphonopropionic acid
- 2-amino-3-phosphopropanoic acid
- 2-AP3
- DL-2-Amino-4-phosphonopropionic acid
- 2-amino-3-(1H-pyrazol-1-yl)propanoic acid
- PIGOPELHGLPKLL-UHFFFAOYSA-N
- A876799
- 3-(Pyrazol-1-yl)-DL-alanine
- 2-amino-3-pyrazol-1-ylpropanoic acid
- (1)-alpha-Amino-1H-pyrazole-1-propionic acid
- EINECS 248-785-0
- SY026507
- SB36358
- EN300-147175
- MFCD09832221
- 2-amino-3-(1H-pyrazol-1-yl)propanoicacid
- FT-0651130
- 28024-60-4
- 1-pyrazolylalanine
- L-2-Amino-3-(1-pyrazolyl)propanoic acid
- FT-0763115
- CHEBI:165849
- AC5797
- AKOS009235513
- A5318
- Pyrazole-1-alanine
- NS00049266
- DTXSID60901786
- SCHEMBL4153679
- Z2933867195
- alpha-Amino-beta-(pyrazolyl-N)propionic acid
- ( inverted exclamation markA)-alpha-amino-1H-pyrazole-1-propionic acid
- 3-(1-Pyrazolyl)-alanine
- 2-amino-3-pyrazol-1-yl-propanoic acid
- propanoic acid, 2-amino-3-(1-pyrazolyl)-
- (+/-)-alpha-amino-1H-pyrazole-1-propionic acid
- DB-067865
- (R)-2-Amino-3-pyrazol-1-yl-propionicacid
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- MDL: MFCD09832221
- Inchi: 1S/C6H9N3O2/c7-5(6(10)11)4-9-3-1-2-8-9/h1-3,5H,4,7H2,(H,10,11)
- InChI Key: PIGOPELHGLPKLL-UHFFFAOYSA-N
- SMILES: OC(C(CN1C=CC=N1)N)=O
Computed Properties
- Exact Mass: 155.06900
- Monoisotopic Mass: 155.069477
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 11
- Rotatable Bond Count: 3
- Complexity: 151
- 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
- Topological Polar Surface Area: 81.1
- XLogP3: -3.4
Experimental Properties
- Density: 1.44
- Boiling Point: 342.8°C at 760 mmHg
- Flash Point: 161.1°C
- Refractive Index: 1.631
- PSA: 81.14000
- LogP: -0.00470
2-amino-3-(1H-pyrazol-1-yl)propanoic acid Customs Data
- HS CODE:2933199090
- Customs Data:
China Customs Code:
2933199090Overview:
2933199090. Other structurally non fused pyrazole ring compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
2-amino-3-(1H-pyrazol-1-yl)propanoic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM124780-1g |
2-amino-3-(1H-pyrazol-1-yl)propanoic acid |
28024-60-4 | 95% | 1g |
$333 | 2021-06-09 | |
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 68R0327-1g |
2-Amino-3-pyrazol-1-yl-propionic acid |
28024-60-4 | 96% | 1g |
3375.21CNY | 2021-05-07 | |
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 68R0327-5g |
2-Amino-3-pyrazol-1-yl-propionic acid |
28024-60-4 | 96% | 5g |
13500.84CNY | 2021-05-07 | |
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 68R0327-500mg |
2-Amino-3-pyrazol-1-yl-propionic acid |
28024-60-4 | 96% | 500mg |
2111.63CNY | 2021-05-07 | |
| Apollo Scientific | OR470698-1g |
2-Amino-3-(1-pyrazolyl)propanoic acid |
28024-60-4 | 1g |
£553.00 | 2023-09-02 | ||
| Chemenu | CM124780-1g |
2-amino-3-(1H-pyrazol-1-yl)propanoic acid |
28024-60-4 | 95% | 1g |
$333 | 2024-07-28 | |
| eNovation Chemicals LLC | D697542-1g |
2-Amino-3-(1-pyrazolyl)propanoic Acid |
28024-60-4 | 95% | 1g |
$715 | 2024-07-20 | |
| Alichem | A049005283-1g |
2-Amino-3-(1H-pyrazol-1-yl)propanoic acid |
28024-60-4 | 95% | 1g |
$400.00 | 2023-09-02 | |
| Enamine | EN300-147175-0.05g |
2-amino-3-(1H-pyrazol-1-yl)propanoic acid |
28024-60-4 | 95% | 0.05g |
$102.0 | 2023-05-03 | |
| Enamine | EN300-147175-0.1g |
2-amino-3-(1H-pyrazol-1-yl)propanoic acid |
28024-60-4 | 95% | 0.1g |
$152.0 | 2023-05-03 |
2-amino-3-(1H-pyrazol-1-yl)propanoic acid Suppliers
2-amino-3-(1H-pyrazol-1-yl)propanoic acid Related Literature
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
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Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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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
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Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
Additional information on 2-amino-3-(1H-pyrazol-1-yl)propanoic acid
Recent Advances in the Study of 2-amino-3-(1H-pyrazol-1-yl)propanoic acid (CAS: 28024-60-4)
The compound 2-amino-3-(1H-pyrazol-1-yl)propanoic acid (CAS: 28024-60-4) has recently garnered significant attention in the field of chemical biology and medicinal chemistry due to its unique structural properties and potential therapeutic applications. This research briefing aims to synthesize the latest findings on this compound, focusing on its synthesis, biological activity, and potential applications in drug development.
Recent studies have highlighted the versatility of 2-amino-3-(1H-pyrazol-1-yl)propanoic acid as a building block for the design of novel bioactive molecules. Its pyrazole moiety, in particular, has been shown to interact with various biological targets, including enzymes and receptors, making it a promising scaffold for drug discovery. Researchers have employed advanced synthetic techniques, such as multi-component reactions and click chemistry, to derivatize this compound and explore its pharmacological potential.
One of the most notable findings in recent literature is the compound's role as a modulator of inflammatory pathways. In vitro and in vivo studies have demonstrated that derivatives of 2-amino-3-(1H-pyrazol-1-yl)propanoic acid exhibit significant anti-inflammatory activity by inhibiting key pro-inflammatory cytokines. This has sparked interest in its potential application for treating chronic inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease.
Additionally, the compound's structural similarity to natural amino acids has led to investigations into its use as a peptide mimetic. Researchers have successfully incorporated 2-amino-3-(1H-pyrazol-1-yl)propanoic acid into peptide sequences, resulting in enhanced stability and bioactivity. This approach has shown promise in the development of peptide-based therapeutics for various conditions, including cancer and metabolic disorders.
From a mechanistic perspective, computational modeling and X-ray crystallography studies have provided valuable insights into the molecular interactions of 2-amino-3-(1H-pyrazol-1-yl)propanoic acid with its biological targets. These structural studies have revealed specific binding modes and key intermolecular interactions that contribute to its biological activity, offering opportunities for structure-based drug design.
Despite these promising developments, challenges remain in optimizing the pharmacokinetic properties of 2-amino-3-(1H-pyrazol-1-yl)propanoic acid derivatives. Current research efforts are focused on improving solubility, metabolic stability, and bioavailability through strategic structural modifications. Recent advances in formulation technologies, such as nanoparticle-based delivery systems, may offer solutions to these challenges.
In conclusion, 2-amino-3-(1H-pyrazol-1-yl)propanoic acid (CAS: 28024-60-4) represents a valuable chemical entity with diverse applications in medicinal chemistry. The growing body of research on this compound underscores its potential as a versatile scaffold for drug discovery and development. Future studies should focus on translating these findings into clinically relevant therapeutics while addressing the current limitations in drug-like properties.
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