Cas no 1246552-38-4 (5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid)

5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid is a heterocyclic compound featuring both amino and carboxylic acid functional groups, making it a versatile intermediate in organic synthesis and pharmaceutical applications. Its pyrazole core structure is valuable for constructing biologically active molecules, particularly in the development of agrochemicals and medicinal compounds. The ethyl substitution at the 1-position enhances stability, while the carboxylic acid and amino groups provide reactive sites for further derivatization. This compound is characterized by high purity and consistent performance, ensuring reliability in research and industrial processes. Its compatibility with a range of reaction conditions makes it a practical choice for synthetic chemists.
5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid structure
1246552-38-4 structure
Product Name:5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid
CAS No:1246552-38-4
MF:C6H9N3O2
MW:155.154560804367
CID:5157894
PubChem ID:53424219
Update Time:2025-06-13

5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 5-AMINO-1-ETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
    • 5-Amino-1-ethyl-pyrazole-4-carboxylic acid
    • 5-Amino-1-ethylpyrazole-4-carboxylic acid
    • AB31623
    • 1H-Pyrazole-4-carboxylic acid, 5-amino-1-ethyl-
    • 5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid
    • Inchi: 1S/C6H9N3O2/c1-2-9-5(7)4(3-8-9)6(10)11/h3H,2,7H2,1H3,(H,10,11)
    • InChI Key: WQBBXOAXPWLRDK-UHFFFAOYSA-N
    • SMILES: OC(C1C=NN(C=1N)CC)=O

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 162
  • XLogP3: 0.3
  • Topological Polar Surface Area: 81.1

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Additional information on 5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid

Comprehensive Overview of 5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid (CAS No. 1246552-38-4)

5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid (CAS No. 1246552-38-4) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This pyrazole derivative is characterized by its unique molecular structure, featuring an amino group and a carboxylic acid moiety, which make it a versatile intermediate in synthetic chemistry. Researchers and industry professionals often search for "pyrazole derivatives in drug discovery" or "5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid applications," reflecting its growing relevance in modern science.

The compound's CAS number 1246552-38-4 serves as a critical identifier in chemical databases, ensuring accurate referencing in patents and academic literature. Its structural features, such as the ethyl-substituted pyrazole ring, contribute to its stability and reactivity, making it a valuable building block for designing novel bioactive molecules. Recent trends in "green chemistry" and "sustainable synthesis" have further highlighted the importance of such intermediates, as they enable efficient routes to reduce waste and energy consumption in industrial processes.

In the context of drug development, 5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid is frequently explored for its potential in creating kinase inhibitors and anti-inflammatory agents. Searches like "pyrazole-based therapeutics" or "CAS 1246552-38-4 in medicinal chemistry" underscore its role in addressing unmet medical needs. Additionally, its compatibility with parallel synthesis techniques aligns with the demand for high-throughput screening in pharmaceutical R&D.

Beyond pharmaceuticals, this compound finds utility in agrochemical formulations, particularly in the synthesis of crop protection agents. Queries such as "pyrazole herbicides" or "1246552-38-4 in agriculture" reflect its cross-disciplinary applications. The carboxylic acid group allows for further functionalization, enabling the development of tailored solutions for pest and disease management.

From a technical perspective, the purity and characterization of 5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid are paramount. Analytical methods like HPLC, NMR, and mass spectrometry are routinely employed to ensure quality control. Researchers often seek "CAS 1246552-38-4 synthesis protocol" or "pyrazole derivative purification," emphasizing the need for standardized procedures in laboratory settings.

In summary, 5-Amino-1-ethyl-1H-pyrazole-4-carboxylic acid (CAS No. 1246552-38-4) represents a pivotal compound in both academic and industrial spheres. Its multifaceted applications, coupled with the rising interest in "heterocyclic chemistry" and "small-molecule drug design," position it as a key player in advancing scientific innovation. Future research may uncover even broader utilities, solidifying its status as a cornerstone in synthetic and applied chemistry.

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