• 1. An integrated chip for immunofluorescence and its application to analyze lysosomal storage disorders
  Jie Shen,Ying Zhou,Tu Lu,Junya Peng,Zhixiang Lin,Yuhong Pang,Li Yu Lab Chip, 2012,12, 317-324
• 2. An alumina stabilized graphene oxide wrapped SnO2 hollow sphere LIB anode with improved lithium storage?
  Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
• 3. An amorphous carbon nitride/NiO/CoN-based composite: a highly efficient nonprecious electrode for supercapacitors and the oxygen evolution reaction?
  Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
• 4. An analyte-triggered artificial peroxidase system based on dimanganese complex for a versatile enzyme assay?
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• 5. An insight into the hybridization mechanism of hairpin DNA physically immobilized on chemically modified graphenes
  Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471

4-amino-N-cyclopentyl-1-methyl-1H-pyrazole-3-carboxamide (CAS No. 906087-57-8): A Comprehensive Overview

4-amino-N-cyclopentyl-1-methyl-1H-pyrazole-3-carboxamide (CAS No. 906087-57-8) is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research. This compound, with its unique pyrazole-carboxamide structure, serves as a crucial intermediate in the synthesis of various bioactive molecules. Its molecular formula is C10H16N4O, and it features a cyclopentyl group attached to the amide nitrogen, which enhances its potential for diverse applications.

The compound's 4-amino substitution on the pyrazole ring makes it a valuable building block in medicinal chemistry. Researchers are particularly interested in its role as a precursor for kinase inhibitors, which are pivotal in targeted cancer therapies. Given the rising global focus on precision medicine and personalized therapeutics, 4-amino-N-cyclopentyl-1-methyl-1H-pyrazole-3-carboxamide is increasingly relevant in drug discovery pipelines.

From a chemical perspective, this compound exhibits moderate solubility in polar organic solvents like dimethyl sulfoxide (DMSO) and methanol, which facilitates its use in laboratory settings. Its stability under ambient conditions makes it suitable for long-term storage, a critical factor for industrial applications. The carboxamide moiety also allows for further functionalization, enabling chemists to tailor its properties for specific needs.

In recent years, the demand for heterocyclic compounds like 4-amino-N-cyclopentyl-1-methyl-1H-pyrazole-3-carboxamide has surged, driven by advancements in combinatorial chemistry and high-throughput screening. These techniques rely heavily on versatile intermediates to accelerate the discovery of novel therapeutics. As such, this compound aligns perfectly with the industry's shift toward faster, more efficient drug development processes.

Another area where this compound shows promise is in the field of agrochemicals. Its structural features are being explored for the design of next-generation pesticides and herbicides, addressing the growing need for sustainable agricultural solutions. With global food security becoming a pressing issue, innovations in crop protection chemicals are more important than ever.

The synthesis of 4-amino-N-cyclopentyl-1-methyl-1H-pyrazole-3-carboxamide typically involves multi-step organic reactions, including amide coupling and cyclization processes. Optimizing these synthetic routes is a key focus for manufacturers aiming to improve yield and reduce costs. Recent publications highlight novel catalytic methods that enhance the efficiency of producing this compound, reflecting the dynamic nature of chemical research.

From a commercial standpoint, the market for pyrazole derivatives is expanding rapidly. Pharmaceutical companies and contract research organizations (CROs) are actively sourcing high-quality 4-amino-N-cyclopentyl-1-methyl-1H-pyrazole-3-carboxamide to support their R&D activities. Suppliers who can ensure consistent purity and scalability are well-positioned to meet this demand.

For researchers working with this compound, proper handling and storage are essential to maintain its integrity. While it is not classified as hazardous, standard laboratory precautions should be followed. Analytical techniques such as HPLC, NMR, and mass spectrometry are commonly employed to verify its purity and structure.

Looking ahead, the versatility of 4-amino-N-cyclopentyl-1-methyl-1H-pyrazole-3-carboxamide ensures its continued relevance in scientific and industrial applications. Whether in drug discovery, agrochemical development, or material science, this compound exemplifies the intersection of innovation and practicality. As the scientific community explores new frontiers, compounds like this will remain at the forefront of cutting-edge research.

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