Cas no 956395-22-5 (1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride)

1-(3-Fluorobenzyl)-1H-pyrazol-4-amine dihydrochloride is a fluorinated pyrazole derivative with applications in pharmaceutical and chemical research. Its dihydrochloride salt form enhances solubility and stability, making it suitable for synthetic and biological studies. The presence of a 3-fluorobenzyl group introduces electron-withdrawing properties, which can influence reactivity in medicinal chemistry applications. This compound serves as a versatile intermediate for the development of heterocyclic compounds, particularly in the synthesis of potential bioactive molecules. Its well-defined structure and high purity ensure reproducibility in experimental settings. Researchers value this compound for its utility in exploring structure-activity relationships and optimizing lead compounds in drug discovery.
1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride structure
956395-22-5 structure
Product Name:1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride
CAS No:956395-22-5
MF:C10H10FN3
MW:191.204905033112
MDL:MFCD02253996
CID:1076681
PubChem ID:6483867
Update Time:2025-11-02

1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-(3-Fluorobenzyl)-1H-pyrazol-4-amine
    • 1-(3-Fluoro-benzyl)-1H-pyrazol-4-ylamine
    • SCHEMBL3616273
    • EN300-228966
    • AKOS000205248
    • 956395-22-5
    • MFCD02253996
    • 1-[(3-fluorophenyl)methyl]-1h-pyrazol-4-amine
    • 1-[(3-fluorophenyl)methyl]pyrazol-4-amine
    • BBL029650
    • STK312459
    • 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride
    • MDL： MFCD02253996
    • Inchi： 1S/C10H10FN3/c11-9-3-1-2-8(4-9)6-14-7-10(12)5-13-14/h1-5,7H,6,12H2
    • InChI Key： DNOLCFDXGUQEQK-UHFFFAOYSA-N
    • SMILES： FC1=CC=CC(=C1)CN1C=C(C=N1)N

Computed Properties

  • Exact Mass: 191.08587549g/mol
  • Monoisotopic Mass: 191.08587549g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 188
  • 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: 1.2
  • Topological Polar Surface Area: 43.8?2

Experimental Properties

  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 365.3±27.0 °C at 760 mmHg
  • Flash Point: 174.7±23.7 °C
  • Vapor Pressure: 0.0±0.8 mmHg at 25°C

1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride Security Information

1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride Pricemore >>

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1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride Related Literature

Additional information on 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride

1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride (CAS No. 956395-22-5): A Comprehensive Overview

1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride (CAS No. 956395-22-5) is a specialized chemical compound that has garnered significant attention in pharmaceutical and biochemical research. This compound, characterized by its unique molecular structure, plays a pivotal role in the development of novel therapeutic agents. Its fluorobenzyl and pyrazole moieties make it a valuable intermediate in medicinal chemistry, particularly in the design of targeted drug molecules.

The growing interest in 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride is driven by its potential applications in addressing contemporary health challenges. Researchers are increasingly exploring its utility in the development of treatments for neurological disorders and inflammatory conditions, which are among the most searched topics in medical and biochemical forums today. The compound's ability to modulate specific biological pathways makes it a promising candidate for next-generation therapeutics.

From a structural perspective, 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride features a pyrazole ring substituted with a 3-fluorobenzyl group and an amine functionality. This configuration enhances its reactivity and binding affinity, making it suitable for various synthetic applications. The dihydrochloride salt form improves its solubility and stability, which are critical factors in pharmaceutical formulations.

In the realm of drug discovery, 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride is often utilized as a building block for more complex molecules. Its incorporation into drug candidates has shown promising results in preclinical studies, particularly in targeting enzymes and receptors associated with chronic diseases. This aligns with the current trend in pharmaceutical research, where there is a high demand for compounds that can address unmet medical needs.

The synthesis of 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride involves multi-step organic reactions, ensuring high purity and yield. Advanced analytical techniques, such as NMR and HPLC, are employed to verify its chemical identity and quality. These rigorous protocols ensure that the compound meets the stringent standards required for research and development purposes.

Market dynamics indicate a rising demand for 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride, driven by the expanding pharmaceutical and biotechnology sectors. Companies specializing in fine chemicals and custom synthesis are increasingly offering this compound to meet the needs of academic and industrial researchers. Its versatility and potential for innovation make it a sought-after material in the scientific community.

In conclusion, 1-(3-Fluorobenzyl)-1h-pyrazol-4-amine Dihydrochloride (CAS No. 956395-22-5) represents a critical component in modern chemical and pharmaceutical research. Its unique properties and broad applicability position it as a key player in the development of new therapeutic solutions. As research continues to uncover its full potential, this compound is expected to remain at the forefront of scientific and medical advancements.

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