Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
25972
CAS Number:
306936-57-2
3-(4-fluorophényl)-1 H -pyrazole-4-carboxaldéhyde
Purity:
≥ 99 % (HPLC)
Documents
$52.88 /250 mg
Taille
Request Bulk Quote
Product Information

3-(4-Fluorophenyl)-1H-pyrazole-4-carboxaldehyde is a versatile compound with significant applications in pharmaceutical research and development. This compound, also known as 4-Fluoro-3-(1H-pyrazol-4-yl)benzaldehyde, is characterized by its unique pyrazole structure, which contributes to its reactivity and potential as a building block in the synthesis of various biologically active molecules. Its fluorinated aromatic ring enhances its lipophilicity, making it an attractive candidate for drug design, particularly in the development of anti-inflammatory and anticancer agents.

Researchers have utilized 3-(4-Fluorophenyl)-1H-pyrazole-4-carboxaldehyde in the synthesis of novel heterocyclic compounds, showcasing its utility in creating targeted therapies. Its ability to act as an intermediate in complex organic syntheses highlights its relevance in medicinal chemistry. Additionally, the compound's distinct properties may offer advantages over similar compounds, such as improved selectivity and potency in biological assays. This makes it a valuable addition to any research laboratory focused on innovative drug discovery and development.

CAS Number
306936-57-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H7FN2O
Molecular Weight
190.18
MDL Number
MFCD01922131
PubChem ID
605439
Melting Point
166-174 ?C
Appearance
Poudre amorphe jaune pâle
Conditions
Conserver à 0-8°C
General Information
CAS Number
306936-57-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H7FN2O
Molecular Weight
190.18
MDL Number
MFCD01922131
PubChem ID
605439
Melting Point
166-174 ?C
Appearance
Poudre amorphe jaune pâle
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(4-Fluorophenyl)-1H-pyrazole-4-carboxaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, contributing to the development of effective pesticides and herbicides that target specific pests while minimizing environmental impact.
  • Material Science: The compound is explored for its potential in creating novel materials, such as polymers and coatings, that exhibit enhanced thermal and chemical resistance.
  • Biochemical Research: It plays a role in studying enzyme interactions and biological pathways, aiding researchers in understanding disease mechanisms and developing targeted therapies.
  • Fluorescent Probes: This chemical is investigated for use in fluorescent probes, which are essential in imaging techniques for cellular and molecular biology, enhancing the visualization of biological processes.

Citations