Cas no 1260891-66-4 (Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate)
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate Chemical and Physical Properties
Names and Identifiers
-
- Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate
- CS-0049242
- PB15159
- 1260891-66-4
- Methyl1H-pyrazolo[4,3-b]pyridine-3-carboxylate
- AMY34144
- MFCD13195415
- DTXSID50855623
- AKOS016000307
- AS-34291
- A889740
- OWIHNHBYZCKVCP-UHFFFAOYSA-N
- SCHEMBL16517165
- 1H-PYRAZOLO[4,3-B]PYRIDINE-3-CARBOXYLIC ACID, METHYL ESTER
- 1H-Pyrazolo[4,3-b]pyridine-3-carboxylic acid methyl ester
- DB-180886
- 1H-Pyrazolo[4,3-b]pyridine-3-carboxylicacid,Methylester
-
- MDL: MFCD13195415
- Inchi: 1S/C8H7N3O2/c1-13-8(12)7-6-5(10-11-7)3-2-4-9-6/h2-4H,1H3,(H,10,11)
- InChI Key: OWIHNHBYZCKVCP-UHFFFAOYSA-N
- SMILES: O(C)C(C1C2=C(C=CC=N2)NN=1)=O
Computed Properties
- Exact Mass: 177.053826475g/mol
- Monoisotopic Mass: 177.053826475g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 13
- Rotatable Bond Count: 2
- Complexity: 210
- 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: 0.8
- Topological Polar Surface Area: 67.9?2
Experimental Properties
- Density: 1.4±0.1 g/cm3
- Boiling Point: 362.9±22.0 °C at 760 mmHg
- Flash Point: 173.3±22.3 °C
- Vapor Pressure: 0.0±0.8 mmHg at 25°C
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| CHENG DOU FEI BO YI YAO Technology Co., Ltd. | FB06338-5g |
methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 95% | 5g |
$1450 | 2023-09-07 | |
| Matrix Scientific | 122614-1g |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate, 97.0% |
1260891-66-4 | 97.0% | 1g |
$1254.00 | 2023-09-07 | |
| Fluorochem | 215131-500mg |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 95% | 500mg |
£315.00 | 2022-02-28 | |
| Fluorochem | 215131-1g |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 95% | 1g |
£473.00 | 2022-02-28 | |
| Fluorochem | 215131-5g |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 95% | 5g |
£1440.00 | 2022-02-28 | |
| Fluorochem | 215131-10g |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 95% | 10g |
£2386.00 | 2022-02-28 | |
| TRC | M335338-10mg |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 10mg |
$ 70.00 | 2022-06-03 | ||
| TRC | M335338-50mg |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 50mg |
$ 230.00 | 2022-06-03 | ||
| TRC | M335338-100mg |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 100mg |
$ 340.00 | 2022-06-03 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | M173104-500mg |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate |
1260891-66-4 | 97% | 500mg |
¥11662.90 | 2023-09-01 |
Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate Related Literature
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Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
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Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre Albrecht Chem. Commun., 2001, 1976-1977
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José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
Additional information on Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate
Exploring the Versatile Applications of Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate (CAS No. 1260891-66-4) in Modern Chemistry
The compound Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate (CAS No. 1260891-66-4) is a heterocyclic organic molecule that has garnered significant attention in pharmaceutical and agrochemical research. Its unique structure, featuring a pyrazolo[4,3-b]pyridine core, makes it a valuable scaffold for designing novel bioactive compounds. Researchers are increasingly exploring its potential as a building block for drug discovery, particularly in targeting enzymes and receptors associated with inflammation and metabolic disorders.
One of the most searched questions about Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate revolves around its synthesis and purification methods. The compound is typically synthesized through multi-step organic reactions, including cyclization and esterification processes. Recent advancements in green chemistry have also led to the development of more sustainable synthetic routes, reducing the environmental impact of its production. This aligns with the growing demand for eco-friendly chemical processes in the industry.
The pyrazolo[4,3-b]pyridine moiety present in this compound has shown remarkable potential in medicinal chemistry. Many researchers are investigating its use as a privileged structure in the design of kinase inhibitors, which are crucial for developing targeted cancer therapies. The ester functional group at the 3-position (carboxylate) provides an excellent handle for further derivatization, allowing medicinal chemists to fine-tune the compound's physicochemical properties and biological activity.
In material science applications, Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate has emerged as a promising candidate for organic electronic materials. Its conjugated system and ability to form stable complexes with various metals make it suitable for developing organic light-emitting diodes (OLEDs) and photovoltaic devices. This application has become particularly relevant as the world shifts toward renewable energy solutions and more efficient display technologies.
The stability and storage conditions of 1260891-66-4 are another frequent topic of inquiry among users. Proper handling requires protection from moisture and extreme temperatures, with recommended storage in airtight containers under inert atmosphere. These precautions ensure the compound maintains its integrity for extended periods, which is essential for research and industrial applications where batch-to-batch consistency is critical.
Recent studies have highlighted the potential of Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate derivatives in addressing antibiotic resistance, a major global health concern. By modifying the core structure, scientists have developed compounds with enhanced antimicrobial activity against resistant bacterial strains. This application has sparked considerable interest in both academic and pharmaceutical circles, particularly in light of the WHO's warnings about the growing threat of superbugs.
Analytical characterization of CAS No. 1260891-66-4 typically involves advanced techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography. These methods provide crucial information about the compound's purity, structure, and conformation, which are essential for quality control in research and production settings. The development of rapid analytical protocols for this compound has been another area of active investigation.
The commercial availability of Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate has improved significantly in recent years, with multiple suppliers offering it in various quantities and purity grades. This increased accessibility has facilitated broader research into its applications across different fields. However, researchers should always verify the quality and authenticity of the compound through proper analytical methods before use in critical experiments.
Looking to the future, the versatility of the pyrazolo[4,3-b]pyridine scaffold suggests that Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate will continue to play an important role in chemical innovation. Its applications span from drug discovery to materials science, addressing some of today's most pressing scientific challenges. As synthetic methodologies advance and our understanding of its properties deepens, we can expect to see even more innovative uses for this remarkable compound emerge in the coming years.
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