Cas no 79068-31-8 (Methyl 3-hydroxy-1H-pyrrole-2-carboxylate)

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate is a heterocyclic ester compound featuring a hydroxyl-substituted pyrrole core. Its structural framework makes it a valuable intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. The presence of both hydroxyl and carboxylate functional groups enhances its reactivity, enabling diverse derivatization pathways. This compound exhibits stability under standard handling conditions and demonstrates compatibility with common organic solvents, facilitating its use in multi-step synthetic routes. Its well-defined molecular structure ensures consistent performance in applications such as ligand design or as a building block for complex heterocyclic systems. The compound is typically supplied with high purity, meeting rigorous analytical standards for research and industrial use.
Methyl 3-hydroxy-1H-pyrrole-2-carboxylate structure
79068-31-8 structure
Product Name:Methyl 3-hydroxy-1H-pyrrole-2-carboxylate
CAS No:79068-31-8
MF:C6H7NO3
MW:141.124681711197
MDL:MFCD11975599
CID:554201
PubChem ID:54711834
Update Time:2025-11-02

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate Chemical and Physical Properties

Names and Identifiers

    • 3-hydroxy-1H-Pyrrole-2-carboxylic acid methyl ester
    • Methyl 3-hydroxy-1H-pyrrole-2-carboxylate
    • 1H-Pyrrole-2-carboxylicacid, 3-hydroxy-, methyl ester
    • Methyl 3-hydroxy-1-H-pyrrole-2-carboxyate
    • 1H-Pyrrole-2-carboxylicacid,3-hydroxy-,methylester(9CI)
    • 3-Hydroxy-2-pyrrolcarbonsaeure-methylester
    • AK123374
    • KB-256492
    • methyl 3-(hydroxy)-1H-pyrrole-2-carboxylate
    • QC-2099
    • SureCN2937272
    • WDPQPKMCONIREA-UHFFFAOYSA-N
    • BCP27565
    • 2368AC
    • AB0095215
    • DS-6996
    • SCHEMBL2937272
    • YSWG258
    • DTXSID30716162
    • METHYL3-HYDROXY-1H-PYRROLE-2-CARBOXYLATE
    • AKOS006351325
    • A15812
    • 79068-31-8
    • CS-0044020
    • 3-hydroxy-1-H-pyrrole-2-carboxy ate
    • SB63895
    • EN300-178432
    • MFCD11975599
    • Methyl 3-hydroxy-1H-pyrrole-2-carboxylate (ACI)
    • MDL: MFCD11975599
    • Inchi: 1S/C6H7NO3/c1-10-6(9)5-4(8)2-3-7-5/h2-3,7-8H,1H3
    • InChI Key: WDPQPKMCONIREA-UHFFFAOYSA-N
    • SMILES: O=C(C1=C(O)C=CN1)OC

Computed Properties

  • Exact Mass: 141.043
  • Monoisotopic Mass: 141.043
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 137
  • 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: 62.3
  • XLogP3: 1.1

Experimental Properties

  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 264.2±20.0 °C at 760 mmHg
  • Flash Point: 113.6±21.8 °C
  • Vapor Pressure: 0.0±0.6 mmHg at 25°C

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate Security Information

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Suzhou Senfeida Chemical Co., Ltd
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(CAS:79068-31-8)1H-Pyrrole-2-carboxylicacid,3-hydroxy-,methylester(9CI)
Order Number:sfd6662
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:34
Price ($):discuss personally

Additional information on Methyl 3-hydroxy-1H-pyrrole-2-carboxylate

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate: A Versatile Compound in Modern Pharmaceutical Research

CAS No. 79068-31-8 is a critical compound in the field of biomedical innovation, with its unique molecular structure and functional groups making it a focal point for researchers exploring drug discovery and biomaterial development. The chemical name Methyl 3-hydroxy-1H-pyrrole-2-carboxylate encapsulates key features that define its chemical behavior and biological relevance. This compound belongs to the class of pyrrole derivatives, which are widely studied for their potential in synthesizing pharmaceutical agents with diverse therapeutic applications.

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate is characterized by the presence of a hydroxyl group at the 3-position and a carboxylate group at the 2-position within the pyrrole ring. These functional groups are pivotal in determining the compound's reactivity and its interactions with biological targets. Recent studies have highlighted the role of hydroxyl groups in modulating hydrophilic interactions, while the carboxylate group contributes to acid-base equilibrium and metal ion coordination in complex environments.

The synthetic pathway of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate has been extensively investigated in recent years. Researchers have employed advanced organic synthesis techniques, such as electrophilic substitution reactions and condensation reactions, to optimize the yield and purity of this compound. A 2023 study published in Journal of Medicinal Chemistry demonstrated the use of asymmetric catalysis to achieve enantioselective synthesis, which is critical for developing chiral pharmaceuticals with enhanced bioavailability.

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate has shown promising potential in antimicrobial research. A 2024 paper in Antimicrobial Agents and Chemotherapy reported that derivatives of this compound exhibit activity against multidrug-resistant bacteria, particularly Staphylococcus aureus and Pseudomonas aeruginosa. The hydroxyl group is believed to enhance the compound's ability to disrupt bacterial cell membranes, while the carboxylate group facilitates interactions with bacterial surface proteins.

In the realm of neuropharmacology, Methyl 3-hydroxy-1H-pyrrole-2-carboxylate has emerged as a candidate for neurodegenerative disease therapy. A 2023 study in Neurochemical Research explored its role in modulating neuroinflammation by targeting microglial activation. The compound's hydroxyl group was found to act as a radical scavenger, reducing oxidative stress in neuronal cells. This finding underscores its potential as a neuroprotective agent in conditions such as Alzheimer's disease and Parkinson's disease.

The application of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate extends beyond pharmaceuticals into biomaterials science. Researchers at the University of Tokyo (2024) have developed biodegradable polymers incorporating this compound, which show controlled degradation rates in physiological environments. The carboxylate group plays a key role in hydrogel formation, enabling the creation of smart drug delivery systems that respond to pH or temperature changes.

Recent advancements in computational chemistry have further enhanced the understanding of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate's properties. A 2024 study published in Chemical Science used density functional theory (DFT) to predict the compound's electronic structure and reactivity patterns. These simulations revealed that the hydroxyl group significantly influences the compound's acid dissociation constant (pKa), which is critical for its solubility and bioavailability in vivo.

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate has also been investigated for its photophysical properties. A 2023 study in Organic Letters demonstrated that the compound exhibits fluorescence under UV excitation, with a maximum emission wavelength of 450 nm. This property makes it a potential candidate for optical imaging agents in biomedical diagnostics. The carboxylate group was found to enhance the compound's photostability, a critical factor for long-term imaging applications.

Despite its promising applications, the synthesis and purification of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate remain challenging. A 2024 review in Green Chemistry highlighted the environmental impact of traditional synthesis methods, prompting researchers to explore green chemistry approaches. Techniques such as microwave-assisted synthesis and solvent-free reactions have been proposed to reduce energy consumption and waste generation during the production process.

In conclusion, Methyl 3-hydroxy-1H-pyrrole-2-carboxylate represents a versatile compound with significant potential in multiple scientific disciplines. Its unique chemical structure and functional groups make it a valuable target for pharmaceutical development, biomaterials engineering, and computational studies. Ongoing research is expected to unlock further applications, solidifying its role as a key player in the advancement of modern science and technology.

Methyl 3-hydroxy-1H-pyrrole-2-carboxylate continues to attract attention as a promising compound in various fields of research. Its unique chemical properties, including the presence of a hydroxyl group and a carboxylate group, contribute to its diverse applications. The compound's potential in pharmaceuticals, particularly in antimicrobial and neuropharmacological contexts, highlights its significance in developing new therapeutic agents. Furthermore, its role in biomaterials science and computational chemistry underscores its versatility and the importance of continued research in these areas.

As the scientific community advances, the exploration of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate is likely to lead to innovative discoveries and practical applications. The compound's ability to interact with biological systems and its potential for modification through synthetic methods make it a valuable asset in the quest for new solutions to complex challenges in medicine and materials science. Ongoing studies are expected to further enhance our understanding of this compound, paving the way for its integration into a wide range of technological and medical innovations.

Overall, the study of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate exemplifies the importance of interdisciplinary research in driving scientific progress. By combining insights from organic chemistry, pharmacology, and materials science, researchers are uncovering new possibilities for this compound. As the field continues to evolve, the potential applications of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate are expected to expand, contributing to advancements in health, technology, and sustainable development.

With its unique properties and diverse applications, Methyl 3-hydroxy-1H-pyrrole-2-carboxylate stands as a testament to the power of chemical innovation. The compound's role in addressing pressing global challenges, such as antimicrobial resistance and neurodegenerative diseases, highlights its significance in modern science. As research progresses, the compound is poised to play an increasingly important role in shaping the future of pharmaceuticals, materials science, and biomedical technologies.

In summary, the exploration of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate is a dynamic and evolving field that promises to deliver groundbreaking advancements. Its potential to contribute to multiple scientific disciplines underscores the importance of continued research and innovation. As scientists continue to unravel the complexities of this compound, its impact on various fields is expected to grow, paving the way for transformative applications in the years to come.

Through the synthesis, characterization, and application of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate, researchers are not only expanding the boundaries of chemical knowledge but also addressing real-world challenges. The compound's versatility and the ongoing efforts to optimize its properties reflect the dedication of the scientific community to advancing human health and technological progress. As the field continues to evolve, the role of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate is set to become even more prominent, driving innovation and discovery in the years ahead.

Ultimately, the study and application of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate exemplify the transformative power of chemical research. By harnessing the unique properties of this compound, scientists are opening new avenues for innovation that have the potential to revolutionize multiple industries and improve the quality of life for people around the world. As the scientific community continues to explore the possibilities of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate, its impact on science and society is expected to grow, marking a significant milestone in the advancement of modern research and development.

With its unique chemical structure and diverse applications, Methyl 3-hydroxy-1H-pyrrole-2-carboxylate stands as a remarkable example of the potential of chemical innovation. The ongoing research into this compound is not only expanding our understanding of chemical properties but also contributing to the development of new solutions to complex problems. As scientists continue to explore the possibilities of Methyl 3-hydroxy-1H-pyrrole-2-carboxylate, its role in advancing science and technology is set to become even more significant, paving the way for future discoveries and innovations.

In conclusion, the exploration of Methyl 3-hydroxy-1H-pyrand-2-carboxylate is a testament to the power of chemical research in driving progress across multiple disciplines. Its potential to address global challenges and its versatility in application highlight the importance of continued innovation. As the scientific community continues to uncover the complexities of this compound, its impact on science and society is expected to grow, marking a significant milestone in the advancement of modern research and development.

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Suzhou Senfeida Chemical Co., Ltd
(CAS:79068-31-8)1H-Pyrrole-2-carboxylicacid,3-hydroxy-,methylester(9CI)
sfd6662
Purity:99.9%
Quantity:200kg
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