Cas no 124004-31-5 (5-Amino-1H-pyrazole-3-carboxylic acid)
5-Amino-1H-pyrazole-3-carboxylic acid Chemical and Physical Properties
Names and Identifiers
-
- 5-Amino-1H-pyrazole-3-carboxylic acid
- 1H-Pyrazole-3-carboxylic acid, 5-amino
- 1H-Pyrazole-3-carboxylicacid, 5-amino-
- 5-amino-1H-pyrazole-3-carboxylic acid
- 3-amino-1H-pyrazole-5-carboxylic acid
- 5-Aminopyrazole-3-carboxylic acid
- 5-AMino-1H-pyrazol-3-carboxylic acid
- 1H-pyrazol-3-carboxylic acid 5-aMino
- Pyrazole-3-carboxylic acid, 5-amino-
- 1H-Pyrazole-5-amino-3-carboxylic acid
- 1H-Pyrazole-3-carboxylicacid,5-amino-(9CI)
- 5-amino-1H-pyrazole-3-carboxylic acid(SALTDATA: FREE)
- MFCD09431136
- 1H-Pyrazole-3-carboxylicacid,5-amino-
- DD-0710
- 124004-31-5
- MFCD09263793
- FT-0645608
- 5-Amino-2H-pyrazole-3-carboxylic acid
- BB 0219953
- AB09167
- AKOS000305944
- 1H-Pyrazole-3-carboxylic acid, 5-amino-
- 3-azanyl-1H-pyrazole-5-carboxylic acid
- SCHEMBL930682
- AKOS005072475
- J-516658
- 5-Amino-1H-pyrazole-3-carboxylicacid
- EN300-82138
- A805184
- 887408-52-8
- AMY16192
- 5-Amino-1H-pyrazole-3-carboxylic acid #
- CS-0054017
- Z275170588
- 5-Amino-1H-pyrazole-3-carboxylic acid, AldrichCPR
- Oprea1_295065
- A1-01432
- BB 0260074
- DTXSID00337489
- BBL038225
- DB-348003
- STK348640
- 5-Amino-1H-pyrazole-3-carboxylicacid-A13351
- ALBB-000317
-
- MDL: MFCD09263793
- Inchi: 1S/C4H5N3O2/c5-3-1-2(4(8)9)6-7-3/h1H,(H,8,9)(H3,5,6,7)
- InChI Key: ICASMSGEUGPHGI-UHFFFAOYSA-N
- SMILES: OC(C1=CC(N)=NN1)=O
Computed Properties
- Exact Mass: 127.03800
- Monoisotopic Mass: 127.038
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 4
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 127
- 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
- Topological Polar Surface Area: 92A^2
- XLogP3: -0.3
Experimental Properties
- Density: 1.677g/cm3
- Boiling Point: 561.2oC at 760 mmHg
- Flash Point: 293.2oC
- Refractive Index: 1.72
- PSA: 92.00000
- LogP: 0.27130
5-Amino-1H-pyrazole-3-carboxylic acid Security Information
- Hazardous Material transportation number:NONH for all modes of transport
- HazardClass:IRRITANT
5-Amino-1H-pyrazole-3-carboxylic 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%
5-Amino-1H-pyrazole-3-carboxylic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| CHENG DOU FEI BO YI YAO Technology Co., Ltd. | JR0020-25g |
3-amino-1h-pyrazole-5-carboxylic Acid |
124004-31-5 | 97% | 25g |
$1300 | 2023-09-07 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A166664-1g |
5-Amino-1H-pyrazole-3-carboxylic acid |
124004-31-5 | 97% | 1g |
¥1006.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A166664-250mg |
5-Amino-1H-pyrazole-3-carboxylic acid |
124004-31-5 | 97% | 250mg |
¥296.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A166664-5g |
5-Amino-1H-pyrazole-3-carboxylic acid |
124004-31-5 | 97% | 5g |
¥2078.90 | 2023-09-04 | |
| Fluorochem | 043878-1g |
3-Amino-1H-pyrazole-5-carboxylic acid |
124004-31-5 | 95% | 1g |
£82.00 | 2022-03-01 | |
| Fluorochem | 043878-5g |
3-Amino-1H-pyrazole-5-carboxylic acid |
124004-31-5 | 95% | 5g |
£247.00 | 2022-03-01 | |
| Fluorochem | 043878-25g |
3-Amino-1H-pyrazole-5-carboxylic acid |
124004-31-5 | 95% | 25g |
£742.00 | 2022-03-01 | |
| Alichem | A049002841-10g |
5-Amino-1H-pyrazole-3-carboxylic acid |
124004-31-5 | 97% | 10g |
$1055.25 | 2023-09-03 | |
| Alichem | A049002841-25g |
5-Amino-1H-pyrazole-3-carboxylic acid |
124004-31-5 | 97% | 25g |
$1656.24 | 2023-09-03 | |
| Alichem | A049002841-100g |
5-Amino-1H-pyrazole-3-carboxylic acid |
124004-31-5 | 97% | 100g |
$3588.52 | 2023-09-03 |
5-Amino-1H-pyrazole-3-carboxylic acid Related Literature
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Xin Fu,Qing-rong Liang,Rong-guang Luo,Yan-shu Li,Xiao-ping Xiao,Lu-lu Yu,Wen-zhe Shan,Guang-qin Fan J. Mater. Chem. B, 2019,7, 3088-3099
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Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
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Kui Wu,Zhihua Yang,Shilie Pan Dalton Trans., 2015,44, 19856-19864
Additional information on 5-Amino-1H-pyrazole-3-carboxylic acid
Recent Advances in the Application of 5-Amino-1H-pyrazole-3-carboxylic acid (CAS: 124004-31-5) in Chemical Biology and Pharmaceutical Research
5-Amino-1H-pyrazole-3-carboxylic acid (CAS: 124004-31-5) is a heterocyclic compound that has garnered significant attention in chemical biology and pharmaceutical research due to its versatile applications as a building block for drug discovery and development. Recent studies have highlighted its potential in the synthesis of novel bioactive molecules, particularly in the areas of kinase inhibition, antimicrobial agents, and anticancer therapeutics. This research brief aims to summarize the latest findings related to this compound, focusing on its chemical properties, synthetic applications, and biological activities.
One of the key areas of interest is the role of 5-Amino-1H-pyrazole-3-carboxylic acid in the design of kinase inhibitors. Kinases are critical targets in the treatment of various diseases, including cancer and inflammatory disorders. Recent research has demonstrated that derivatives of this compound exhibit potent inhibitory activity against specific kinases, such as cyclin-dependent kinases (CDKs) and Janus kinases (JAKs). For instance, a 2023 study published in the Journal of Medicinal Chemistry reported the synthesis of a series of pyrazole-based CDK inhibitors, with 5-Amino-1H-pyrazole-3-carboxylic acid serving as a core scaffold. These inhibitors showed promising antitumor activity in preclinical models, underscoring the compound's potential in oncology drug development.
In addition to its applications in kinase inhibition, 5-Amino-1H-pyrazole-3-carboxylic acid has been explored for its antimicrobial properties. A recent study in Bioorganic & Medicinal Chemistry Letters (2024) described the synthesis of pyrazole-carboxylic acid hybrids with enhanced antibacterial activity against multidrug-resistant strains. The study revealed that the incorporation of this compound into hybrid molecules significantly improved their binding affinity to bacterial targets, such as DNA gyrase and topoisomerase IV. These findings suggest that 5-Amino-1H-pyrazole-3-carboxylic acid could play a pivotal role in addressing the global challenge of antibiotic resistance.
Another noteworthy application of this compound is in the field of anticancer drug discovery. Researchers have utilized 5-Amino-1H-pyrazole-3-carboxylic acid as a precursor for the synthesis of small molecules that target tumor-specific pathways. For example, a 2024 study in the European Journal of Medicinal Chemistry demonstrated that pyrazole-based compounds derived from this scaffold exhibited selective cytotoxicity against cancer cells while sparing normal cells. The study attributed this selectivity to the compound's ability to modulate reactive oxygen species (ROS) levels and induce apoptosis in malignant cells. These results highlight the compound's potential as a lead structure for the development of next-generation anticancer agents.
From a synthetic chemistry perspective, 5-Amino-1H-pyrazole-3-carboxylic acid offers several advantages, including its stability, ease of functionalization, and compatibility with diverse reaction conditions. Recent advancements in synthetic methodologies have enabled the efficient modification of this compound to yield a wide array of derivatives with tailored biological activities. For instance, a 2023 publication in Organic Letters detailed a novel one-pot synthesis route for pyrazole-carboxylic acid derivatives, which significantly reduced the number of steps and improved overall yields. Such innovations are expected to accelerate the exploration of this compound's full potential in drug discovery.
In conclusion, 5-Amino-1H-pyrazole-3-carboxylic acid (CAS: 124004-31-5) continues to be a valuable scaffold in chemical biology and pharmaceutical research. Its applications span multiple therapeutic areas, including kinase inhibition, antimicrobial therapy, and anticancer drug development. Recent studies have not only expanded our understanding of its biological activities but also advanced synthetic strategies to harness its full potential. As research in this field progresses, this compound is likely to remain a focal point for the discovery of novel therapeutic agents.
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