203000-48-0 Usage
Uses
Used in Chemical Synthesis:
(S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE BIS(BORANE) is used as a reagent and catalyst in various chemical reactions for its ability to facilitate reactions under mild conditions and its compatibility with a wide range of functional groups.
Used in Asymmetric Hydrogenation:
In the field of asymmetric hydrogenation, (S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE BIS(BORANE) is used as a catalyst to selectively reduce certain compounds, which is crucial for the production of enantiomerically pure compounds in pharmaceuticals and other industries.
Used as a Reducing Agent:
(S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE BIS(BORANE) is utilized as a reducing agent in organic synthesis, where it helps in the conversion of functional groups to their reduced forms, which is essential for the synthesis of various organic compounds.
Used in Organometallic Chemistry Research:
In the realm of organometallic chemistry, (S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE BIS(BORANE) is used as a key reagent for studying and developing new reactions and catalytic systems, contributing to the advancement of synthetic methodologies.
Used in Industrial Applications:
(S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE BIS(BORANE) is employed in industrial processes where its reactivity and stability are advantageous for the large-scale production of chemicals, pharmaceuticals, and other related products.
Check Digit Verification of cas no
The CAS Registry Mumber 203000-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,0,0 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 203000-48:
(8*2)+(7*0)+(6*3)+(5*0)+(4*0)+(3*0)+(2*4)+(1*8)=50
50 % 10 = 0
So 203000-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H28P2.2BH3/c1-11(2,3)13(7)9-10-14(8)12(4,5)6;;/h9-10H2,1-8H3;2*1H3/t13-,14-;;/m0../s1
203000-48-0Relevant academic research and scientific papers
Stereospecific construction of a trans-1,4-diphosphacyclohexane skeleton
Morisaki, Yasuhiro,Imoto, Hiroaki,Ouchi, Yuko,Nagata, Yuuya,Chujo, Yoshiki
supporting information; experimental part, p. 1489 - 1492 (2009/05/11)
(Chemical Equation Presented) trans-1,4-Diphosphacyclohexanes were successfully synthesized by the stereospecific intramolecular coupling reaction of the optically active bisphosphine. This is a new route for the construction of the trans-1,4-diphosphacyclohexane skeleton. A cis isomer was also prepared along with the trans isomer from a mixture of rac- and meso-bisphosphines. The coordinated boranes were easily removed to afford the corresponding 1,4-diphosphacyclohexanes.
