Tris(3-methoxyphenyl)phosphine
95%
- Product Code: 121814
Alias:
Tris(3-methoxyphenyl)phosphine
CAS:
29949-84-6
Molecular Weight: | 352.36 g./mol | Molecular Formula: | CH₃OC₆H₄₃P |
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EC Number: | MDL Number: | MFCD00008386 | |
Melting Point: | 113-115 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature, dry |
Product Description:
Tris(3-methoxyphenyl)phosphine is primarily used as a ligand in coordination chemistry, particularly in the synthesis of transition metal complexes. These complexes are often employed as catalysts in various organic reactions, including cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, which are essential in the production of pharmaceuticals and fine chemicals. The methoxy groups on the phenyl rings enhance the electron-donating properties of the phosphine, making it effective in stabilizing metal centers and improving catalytic activity. Additionally, it is utilized in the development of organic light-emitting diodes (OLEDs) and other optoelectronic materials, where it helps in the formation of efficient phosphorescent complexes. Its role in these applications underscores its importance in both industrial and academic research.
Product Specification:
Test | Specification |
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Purity (%) | 94.5-100 |
Appearance | White To Off-White Powder Or Crystals |
Infrared Spectrum | Conforms To Structure |
Proton Nmr Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿320.00 |
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5.000 | 10-20 days | ฿1,300.00 |
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25.000 | 10-20 days | ฿5,780.00 |
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100.000 | 10-20 days | ฿21,460.00 |
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Tris(3-methoxyphenyl)phosphine
Tris(3-methoxyphenyl)phosphine is primarily used as a ligand in coordination chemistry, particularly in the synthesis of transition metal complexes. These complexes are often employed as catalysts in various organic reactions, including cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, which are essential in the production of pharmaceuticals and fine chemicals. The methoxy groups on the phenyl rings enhance the electron-donating properties of the phosphine, making it effective in stabilizing metal centers and improving catalytic activity. Additionally, it is utilized in the development of organic light-emitting diodes (OLEDs) and other optoelectronic materials, where it helps in the formation of efficient phosphorescent complexes. Its role in these applications underscores its importance in both industrial and academic research.
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