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Catalog Number:
18771
CAS Number:
182923-55-3
2-Phenyl-5-trifluoromethyl-2H-pyrazol-3-ylamine
Purity:
≥ 96% (Assay)
Documents
$134.70 /25MG
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Product Information

2-Phenyl-5-trifluoromethyl-2H-pyrazol-3-ylamine is a versatile compound recognized for its unique trifluoromethyl group, which enhances its chemical reactivity and stability. This compound is particularly valuable in pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its structure allows for modifications that can lead to the discovery of new therapeutic agents, especially in the fields of oncology and anti-inflammatory treatments. Additionally, the presence of the phenyl group contributes to its potential as a ligand in coordination chemistry, making it useful in catalysis and material science applications.

Researchers appreciate the compound's ability to facilitate the development of novel compounds with improved efficacy and selectivity. Its unique properties make it an attractive candidate for further exploration in medicinal chemistry, where it can be employed to create targeted therapies. With its growing relevance in various scientific domains, 2-Phenyl-5-trifluoromethyl-2H-pyrazol-3-ylamine stands out as a promising compound for innovative research and development.

CAS Number
182923-55-3
Purity
≥ 96% (Assay)
Molecular Formula
C10H8F3N3
Molecular Weight
227.19
MDL Number
MFCD06738296
PubChem ID
43158951
Appearance
Pale yellow solid
Conditions
Store at 0-8 °C
General Information
CAS Number
182923-55-3
Purity
≥ 96% (Assay)
Molecular Formula
C10H8F3N3
Molecular Weight
227.19
MDL Number
MFCD06738296
PubChem ID
43158951
Appearance
Pale yellow solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Phenyl-5-trifluoromethyl-2H-pyrazol-3-ylamine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-inflammatory and analgesic drugs.
  • Agricultural Chemistry: It is used in formulating agrochemicals, including herbicides and fungicides, enhancing crop protection with its effective biological activity.
  • Material Science: The compound is explored in creating advanced materials, particularly in coatings and polymers, due to its unique chemical properties that improve durability and resistance.
  • Biochemical Research: It acts as a valuable tool in biochemical assays and studies, aiding researchers in understanding enzyme interactions and metabolic pathways.
  • Fluorine Chemistry: The trifluoromethyl group in this compound provides distinctive reactivity, making it a subject of interest in synthetic organic chemistry for creating novel fluorinated compounds.

Citations