263563-97-9 Usage
Uses
Used in Organic Synthesis:
(±)-tert-butylmethylphosphine borane is used as a reducing agent for facilitating the addition of hydrogen to unsaturated organic compounds, making it a valuable reagent in various chemical reactions.
Used in Reduction of Carbonyl Compounds:
(±)-tert-butylmethylphosphine borane is used as a reagent in the reduction of carbonyl compounds, which is an important process in the synthesis of various organic compounds.
Used in Catalyst Applications:
(±)-tert-butylmethylphosphine borane is used as a catalyst in various organic reactions, enhancing the efficiency and selectivity of these processes.
Used in Precursor to Other Boron-Containing Compounds:
(±)-tert-butylmethylphosphine borane is used as a precursor to other boron-containing compounds, contributing to the development of new materials and chemical processes.
Used in Organoboron Chemistry:
(±)-tert-butylmethylphosphine borane is used in the field of organoboron chemistry due to its unique structure and reactivity, making it an important compound for research and development in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 263563-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,5,6 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 263563-97:
(8*2)+(7*6)+(6*3)+(5*5)+(4*6)+(3*3)+(2*9)+(1*7)=159
159 % 10 = 9
So 263563-97-9 is a valid CAS Registry Number.
263563-97-9Relevant academic research and scientific papers
Birch reduction of aryldialkylphosphine-boranes
Stankevi?, Marek,Micha? Pietrusiewicz
supporting information; experimental part, p. 7093 - 7095 (2010/03/03)
Aryldialkylphosphine-boranes undergo facile Birch-type reduction to afford cyclohexadienyldialkylphosphine-boranes in high yields. Judicious choice of the metal and the reaction conditions allows for complete elimination of the undesired P-Ph bond cleavag
Synthesis and enantioselectivity of P-chiral phosphine ligands with alkynyl groups
Imamoto, Tsuneo,Saitoh, Youichi,Koide, Aya,Ogura, Tomokazu,Yoshida, Kazuhiro
, p. 8636 - 8639 (2008/09/18)
(Formula Presented) A range of asymmetric transformations are catalyzed by transition-metal complexes of the title ligands with excellent enantioselectivities. The ligands, which were applied successively in Rh-catalyzed hydrogenation and Rh- or Pd-cataly
