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Catalog Number:
40758
CAS Number:
628333-86-8
1-[2-(Di-tert-butylphosphino)phenyl]-3,5-diphenyl-1H-pyrazole
Purity:
≥ 98% (GC)
Synonym(s):
TrippyPhos
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Product Information

1-[2-(Di-tert-butylphosphino)phenyl]-3,5-diphenyl-1H-pyrazole is a versatile compound known for its unique phosphine functionality, making it an essential reagent in various chemical syntheses. This compound exhibits excellent stability and reactivity, which are crucial for applications in catalysis, particularly in transition metal-catalyzed reactions. Its structure allows for effective coordination with metals, enhancing catalytic efficiency in processes such as cross-coupling reactions and other organic transformations. Researchers and industry professionals can leverage its properties to develop more efficient synthetic pathways, ultimately leading to higher yields and reduced reaction times.

In addition to its catalytic applications, this compound serves as a valuable ligand in coordination chemistry, facilitating the formation of metal complexes that are pivotal in materials science and medicinal chemistry. Its ability to stabilize metal centers while providing unique electronic properties makes it suitable for applications in drug discovery and the development of advanced materials. With its robust performance and adaptability, 1-[2-(Di-tert-butylphosphino)phenyl]-3,5-diphenyl-1H-pyrazole stands out as a key player in modern chemical research and industrial applications.

Synonyms
TrippyPhos
CAS Number
628333-86-8
Purity
≥ 98% (GC)
Molecular Formula
C29H33N2P
Molecular Weight
440.57
MDL Number
MFCD09038823
PubChem ID
11430600
Melting Point
140 - 144 °C
Appearance
White to off-white crystal
Conditions
Store at RT
General Information
Synonyms
TrippyPhos
CAS Number
628333-86-8
Purity
≥ 98% (GC)
Molecular Formula
C29H33N2P
Molecular Weight
440.57
MDL Number
MFCD09038823
PubChem ID
11430600
Melting Point
140 - 144 °C
Appearance
White to off-white crystal
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-[2-(Di-tert-butylphosphino)phenyl]-3,5-diphenyl-1H-pyrazole is widely utilized in research focused on:

  • Catalysis: This compound serves as a highly effective ligand in catalytic processes, particularly in cross-coupling reactions. Its unique structure enhances reaction efficiency, making it valuable in the synthesis of complex organic molecules.
  • Pharmaceutical Development: It plays a crucial role in the design of new pharmaceutical agents. Researchers leverage its properties to develop compounds with improved efficacy and selectivity in targeting specific biological pathways.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.
  • Environmental Chemistry: It is applied in the remediation of pollutants, where its phosphine functionality aids in the extraction and stabilization of heavy metals from contaminated sites.
  • Research in Organometallic Chemistry: This compound is integral in the study of organometallic complexes, providing insights into bonding and reactivity that are essential for advancing this field.

Citations