782501-07-9 Usage
Uses
Used in Coordination Chemistry:
3,5-di-tert-butyl-4-methoxyphenylphosphine is used as a ligand for stabilizing and activating transition metal complexes. Its bulky substituents offer steric protection, enhancing the stability and reactivity of metal complexes in various chemical reactions.
Used in Organometallic Catalysis:
In organometallic catalysis, 3,5-di-tert-butyl-4-methoxyphenylphosphine serves as a ligand to improve the efficiency and selectivity of catalytic processes. Its steric properties allow for better control over the reaction pathways, leading to improved yields and reduced side reactions.
Used in Pharmaceutical Research:
3,5-di-tert-butyl-4-methoxyphenylphosphine is utilized in the synthesis of complex organic molecules with potential pharmaceutical applications. Its ability to stabilize metal complexes can facilitate the development of new drugs and drug delivery systems.
Used in Materials Science Research:
This phosphine ligand is also employed in materials science research, where it can contribute to the design and synthesis of novel materials with unique properties. Its role in stabilizing metal complexes can be leveraged to create advanced materials for various applications, such as sensors, catalysts, and electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 782501-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,2,5,0 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 782501-07:
(8*7)+(7*8)+(6*2)+(5*5)+(4*0)+(3*1)+(2*0)+(1*7)=159
159 % 10 = 9
So 782501-07-9 is a valid CAS Registry Number.
782501-07-9Relevant academic research and scientific papers
Enantioselective acylation using a second-generation P-aryl-2- phosphabicyclo[3.3.0]octane catalyst
MacKay, James A.,Vedejs, Edwin
, p. 6934 - 6937 (2007/10/03)
The synthesis of P-aryl-2-phosphabicylco[3.3.0]-octane·HBF 4 salts 3a and 3c is described. Incorporation of the P-3,5-di-tert-butyl-4-methoxyphenyl group in 3c allows use of a less expensive aryl bromide starting material. Deprotonation of the air-stable salts in situ with triethylamine releases the corresponding phosphines 1a and 1c for use in the kinetic resolution of representative secondary alcohols. The method is convenient for small-scale experiments and affords enantioselectivities s close to the values obtained using the free phosphines 1a and 1b in cases where s is ca. 40 or lower.
