Reaction
ChemicalBook > CAS DataBase List > (R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE

(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE

Reaction
(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE Structure
(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE
  • CAS No.192463-40-4
  • Chemical Name:(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE
  • CBNumber:CB1224685
  • Molecular Formula:C40H34P2
  • Formula Weight:576.65
  • MOL File:192463-40-4.mol
(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE Property
  • Melting point 222-225°C
  • alpha +63.2° (c 3.27, CH2Cl2)
  • storage temp. under inert gas (nitrogen or Argon) at 2-8°C
  • form solid
  • color white
  • optical activity [α]22/D +34°, c = 1 in chloroform
  • CAS DataBase Reference 192463-40-4
  • UNSPSC Code 12352002
  • NACRES NA.22
Safety
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H302-H315-H319-H335
  • Precautionary statements P261-P305+P351+P338
(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE Price More Price(2)
  • Brand: Sigma-Aldrich(India)
  • Product number: 682136
  • Product name : (S)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane
  • Purity: 96%
  • Packaging: 100MG
  • Price: ₹8281.13
  • Updated: 2022/06/14
  • Buy: Buy
  • Brand: Sigma-Aldrich(India)
  • Product number: 682136
  • Product name : (S)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane
  • Purity: 96%
  • Packaging: 500MG
  • Price: ₹33871.43
  • Updated: 2022/06/14
  • Buy: Buy

(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE Chemical Properties,Usage,Production

  • Reaction
    1. Ligand for rhodium-catalyzed enantioselective hydroboration of cyclopropenes.
    2. Ligand for iridium-catalyzed enantioselective [2+2] cycloaddition of oxabicyclic alkenes with terminal alkynes.
    3. Ligand for the palladium-catalyzed enantioselective hydroxycarbonylation and alkoxycarbonylation of alkenes.
    4. Ligand for the palladium-catalyzed amides synthesis via C(sp3 )–H bond functionalization and CO insertion.
    5. Ligand for iridium-catalyzed diene hydrohydroxymethylation.
    Reactions of 192463-40-4
  • Uses Efficient ligand for asymmetric hydrogentation of dehydroamino acids, methyl esters and keytones.
(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE Preparation Products And Raw materials
Raw materials
Preparation Products
(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE Suppliers
Global(44)Suppliers
  • Supplier:
    Coresyn Pharmatech Co., Ltd.
  • Tel:+86-571-86626709<br/>+86-18157142896
  • Email:cbc@coresyn.com
  • Country:China
  • ProdList:9984
  • Advantage:58
  • Supplier:
    Aladdin Scientific
  • Tel:
  • Email:tp@aladdinsci.com
  • Country:United States
  • ProdList:57505
  • Advantage:58
  • Supplier: J & K SCIENTIFIC LTD.
  • Tel: 18210857532
  • Email:jkinfo@jkchemical.com
  • Country:China
  • ProdList:96815
  • Advantage:76
  • Supplier: Alfa Aesar
  • Tel:400-6106006
  • Email:saleschina@alfa-asia.com
  • Country:China
  • ProdList:30123
  • Advantage:84
  • Supplier: Energy Chemical
  • Tel:021-021-58432009<br/>400-005-6266
  • Email:sales8178@energy-chemical.com
  • Country:China
  • ProdList:44732
  • Advantage:61
  • Supplier: Bide Pharmatech Ltd.
  • Tel:400-164-7117<br/>13681763483
  • Email:product02@bidepharm.com
  • Country:China
  • ProdList:41457
  • Advantage:60
(R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE Spectrum
192463-40-4, (R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANERelated Search:
  • organophosphine ligand
  • PHANEPhos Series
  • Chiral Phosphine
  • 高端化学
  • 有机配体
  • 膦配体
  • Chiral Catalysts, Ligands, and Reagents
  • Asymmetric Synthesis
  • Hydrogenation
  • (S)-4,12-双(二苯基膦)-[2.2]二聚对二甲苯
  • (S)-4,12-双(二苯基膦)-[2.2]二聚对二甲苯【大包装请详询客服】
  • (S)-(+)-4,12-双(二苯基膦)-[2.2]-对环芳烷
  • (S)-4,12-二(二苯基膦基)[2.2]对环芳烷,98%,E
  • (S)-4,12-二(二苯基膦)溴[2.2]对环芳,98%,EE98%
  • (S)-4,12-二(二苯基膦)溴[2.2]对环芳
  • (S)-4,12-二(二苯基膦)溴[2.2]对环芳,98%,E
  • (S)-4,12-二(二苯基膦)[2.2]对环芳
  • (S)-4,12-双(二苯基膦)溴[2.2]对环芳烷
  • (S)-4,12-二(二苯基膦基)[2.2]对环芳烷
  • 192463-40-4
  • (<i>S</i>)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane
  • (S)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane, min. 95%,99%ee
  • (S)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane, min. 95%
  • (S)-4,12-Bis(diphenylphosphino)-[2.2]paracyclophane,99%e.e.
  • (Sp)-Phanephos
  • (Sp)-(+)-4,12-Bis(diphenylphosphino)[2.2]paracyclophane
  • (S)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane, min. 97% (S)-PHANEPHOS
  • (S)-(+)-4,12-Bis(D
  • (S)-Phanephos, 98%, ee 98%
  • (S)-(+)-4,12-BIS-(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE (S)-PHANEPHOS
  • (S)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane,min.95%(S)-PHANEPHOS
  • (s)-phanephos
  • 4-FLUOROBENZOYLACETONITRILE, 97% N-BOC-4-OXO-L-PROLINE, 97%
  • Bisdiphenylphosphinoparacyclophane
  • (R)-(-)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE
  • (R)-PHANEPHOS
  • (S)-(+)-4,12-BIS(DIPHENYLPHOSPHINO)-[2.2]-PARACYCLOPHANE