Di-tert-butylchlorophosphine

96%

  • Product Code: 122044
  Alias:    Di-tert-butylphosphine chloride
  CAS:    13716-10-4
Molecular Weight: 180.66 g./mol Molecular Formula: C₈H₁₈ClP
EC Number: MDL Number: MFCD00008815
Melting Point: 2-3°C Boiling Point: 48 °C3 mm Hg(lit.)
Density: 0.951 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: Di-tert-butylchlorophosphine is primarily used as a precursor or reagent in the synthesis of organophosphorus compounds. It is particularly valuable in the preparation of phosphine ligands, which are essential in coordination chemistry and catalysis. These ligands are often employed in transition metal-catalyzed reactions, such as cross-coupling reactions, hydrogenation, and hydroformylation, due to their ability to stabilize metal centers and modulate reactivity. Additionally, this compound is utilized in the development of phosphorus-containing polymers and materials, which can have applications in flame retardants, adhesives, and coatings. Its sterically bulky tert-butyl groups make it useful for creating highly selective and sterically hindered phosphine derivatives, which are important in asymmetric synthesis and fine chemical production.
Product Specification:
Test Specification
Purity (GC) 96-100
Refractive Index N20/D 1.481-1.485
Appearance Colorless Or Yellow Liquid
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿410.00
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5.000 10-20 days ฿1,360.00
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-
25.000 10-20 days ฿5,490.00
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-
100.000 10-20 days ฿21,360.00
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Di-tert-butylchlorophosphine
Di-tert-butylchlorophosphine is primarily used as a precursor or reagent in the synthesis of organophosphorus compounds. It is particularly valuable in the preparation of phosphine ligands, which are essential in coordination chemistry and catalysis. These ligands are often employed in transition metal-catalyzed reactions, such as cross-coupling reactions, hydrogenation, and hydroformylation, due to their ability to stabilize metal centers and modulate reactivity. Additionally, this compound is utilized in the development of phosphorus-containing polymers and materials, which can have applications in flame retardants, adhesives, and coatings. Its sterically bulky tert-butyl groups make it useful for creating highly selective and sterically hindered phosphine derivatives, which are important in asymmetric synthesis and fine chemical production.
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