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Catalog Number:
31875
CAS Number:
564483-19-8
tBuXPhos
Purity:
≥ 98 % (dosage)
Synonym(s):
2-Di- tert -butylphosphino-2',4',6'-triisopropylbiphényle, t-Bu Xphos, tert-butyle Xphos
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Product Information

Ligand efficace pour l'arylation catalysée par le Pd des pyrazoles, des indazoles et des hétérocycles aminés.

Synonyms
2-Di- tert -butylphosphino-2',4',6'-triisopropylbiphényle, t-Bu Xphos, tert-butyle Xphos
CAS Number
564483-19-8
Purity
≥ 98 % (dosage)
Molecular Formula
C 29 H 45 P
Molecular Weight
424.65
MDL Number
MFCD06411306
PubChem ID
11618717
Melting Point
147 - 151 °C
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0 - 8 ºC
General Information
Synonyms
2-Di- tert -butylphosphino-2',4',6'-triisopropylbiphényle, t-Bu Xphos, tert-butyle Xphos
CAS Number
564483-19-8
Purity
≥ 98 % (dosage)
Molecular Formula
C 29 H 45 P
Molecular Weight
424.65
MDL Number
MFCD06411306
PubChem ID
11618717
Melting Point
147 - 151 °C
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0 - 8 ºC
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

tBuXPhos is widely utilized in research focused on:

  • Catalysis: This compound serves as a highly effective ligand in various catalytic reactions, particularly in palladium-catalyzed cross-coupling processes. Its steric properties enhance reaction selectivity and yield.
  • Organic Synthesis: Researchers leverage tBuXPhos for synthesizing complex organic molecules, benefiting from its ability to stabilize reactive intermediates and improve reaction rates.
  • Pharmaceutical Development: In the pharmaceutical industry, it aids in the development of new drugs by facilitating the formation of carbon-carbon bonds, which is crucial for constructing diverse molecular architectures.
  • Material Science: The compound is also applied in the development of advanced materials, including polymers and nanomaterials, due to its unique electronic properties and ability to enhance material performance.
  • Green Chemistry: tBuXPhos contributes to more sustainable practices by enabling reactions that require milder conditions, thus reducing the environmental impact compared to traditional methods.

Citations