T-Butyldicyclohexylphosphine

98%

Reagent Code: #68953
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CAS Number 93634-87-8

science Other reagents with same CAS 93634-87-8

blur_circular Chemical Specifications

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Weight 254.4 g/mol
Formula C₁₆H₃₁P
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

Used as a ligand in transition metal catalysis, particularly in cross-coupling reactions like Suzuki-Miyaura and Heck reactions. It enhances catalytic efficiency due to its steric bulk and electron-donating properties. Commonly applied in pharmaceutical synthesis for constructing complex organic molecules. Also employed in materials science for developing advanced polymers and nanomaterials. Its stability and reactivity make it valuable in asymmetric synthesis for producing enantiomerically pure compounds.

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Test Parameter Specification
Appearance Colorless Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,332.00
inventory 5g
10-20 days ฿15,102.00
inventory 1g
10-20 days ฿3,546.00

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T-Butyldicyclohexylphosphine
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Used as a ligand in transition metal catalysis, particularly in cross-coupling reactions like Suzuki-Miyaura and Heck reactions. It enhances catalytic efficiency due to its steric bulk and electron-donating properties. Commonly applied in pharmaceutical synthesis for constructing complex organic molecules. Also employed in materials science for developing advanced polymers and nanomaterials. Its stability and reactivity make it valuable in asymmetric synthesis for producing enantiomerically pure compound

Used as a ligand in transition metal catalysis, particularly in cross-coupling reactions like Suzuki-Miyaura and Heck reactions. It enhances catalytic efficiency due to its steric bulk and electron-donating properties. Commonly applied in pharmaceutical synthesis for constructing complex organic molecules. Also employed in materials science for developing advanced polymers and nanomaterials. Its stability and reactivity make it valuable in asymmetric synthesis for producing enantiomerically pure compounds.

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