193699-33-1 Usage
Uses
Used in Asymmetric Catalysis:
Binap-Phos is utilized as a chiral ligand in asymmetric catalysis for its ability to promote enantioselective transformations. It is particularly effective in asymmetric hydrogenation and other metal-catalyzed reactions, playing a crucial role in the production of complex organic molecules with high levels of chirality.
Used in Organic Synthesis:
In the field of organic synthesis, Binap-Phos is employed as a key component in various reactions, enhancing the efficiency and selectivity of the processes. Its unique structure and stereocontrolling properties make it a popular choice among synthetic chemists working on challenging transformations, contributing to the development of novel compounds and materials.
Used in Pharmaceutical Industry:
Binap-Phos is also used in the pharmaceutical industry for the synthesis of chiral drugs. Its ability to facilitate enantioselective transformations is invaluable in producing the desired enantiomers of pharmaceutical compounds, which can have significant implications for the efficacy and safety of the final drug product.
Used in Chemical Research:
In academic and industrial research settings, Binap-Phos is a valuable asset for chemists exploring new reaction pathways and developing innovative synthetic methods. Its versatility and effectiveness in promoting enantioselective transformations make it a go-to ligand for researchers working on the cutting edge of chemical science.
Check Digit Verification of cas no
The CAS Registry Mumber 193699-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,9 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 193699-33:
(8*1)+(7*9)+(6*3)+(5*6)+(4*9)+(3*9)+(2*3)+(1*3)=191
191 % 10 = 1
So 193699-33-1 is a valid CAS Registry Number.
193699-33-1Relevant academic research and scientific papers
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8'-methoxy-1,1'-binaphthyl
Fuji, Kaoru,Sakurai, Minoru,Kinoshita, Takayoshi,Kawabata, Takeo
, p. 6323 - 6326 (2007/10/03)
A new chiral monodentate ligand, 8-diphenylphosphino-8'-methoxy-1,1'- binaphthyl (8MeO-MOP), was used for palladium-catalyzed reduction of allylic carbonates with formic acid. Various methylcarbonates of 3,3'-disubstituted allylic alcohols were converted
