| Name | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl |
| Synonyms | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl dicyclohexyl(2',6'-diisopropoxybiphenyl-2-yl)phosphine 2-DicyclohexylphosphiNA-2',6'-diisopropoxy-1,1'-biphenyl 2-Dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl 2-Dicyclohexylphosphino-2',6'-diisopropoxy-1,1'-biphenyl Dicyclohexyl-[2-[2,6-di(propan-2-yloxy)phenyl]phenyl]phosphane {2-[2,6-bis(propan-2-yloxy)phenyl]phenyl}dicyclohexylphosphane Dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine 2-Dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl,RuPhos [2',6'-bis(1-methylethoxy)biphenyl-2-yl](dicyclohexyl)phosphane |
| CAS | 787618-22-8 |
| EINECS | 616-653-5 |
| InChI | InChI=1/C30H43O2P/c1-22(2)31-27-19-13-20-28(32-23(3)4)30(27)26-18-11-12-21-29(26)33(24-14-7-5-8-15-24)25-16-9-6-10-17-25/h11-13,18-25H,5-10,14-17H2,1-4H3 |
| InChIKey | MXFYYFVVIIWKFE-UHFFFAOYSA-N |
| Molecular Formula | C30H43O2P |
| Molar Mass | 466.64 |
| Melting Point | 123-124°C |
| Boling Point | 551.7±40.0 °C(Predicted) |
| Flash Point | 360.7°C |
| Solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) |
| Vapor Presure | 1.18E-11mmHg at 25°C |
| Appearance | Powder |
| Color | white |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Sensitive | Air Sensitive |
| MDL | MFCD06798294 |
| Use | Bulky phosphine ligand used in a palladium-catalyzed cross-coupling of aminoethyltrifluoroborate?s with electron-poor aryl bromides. |
| Hazard Symbols | Xn - Harmful![]() |
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| WGK Germany | 3 |
| TSCA | No |
| HS Code | 29310099 |
| Introduction | 2-dicyclohexylphosphine -2 ',6'-diisopropoxy-1, 1 '-biphenyl is a hydrocarbon derivative and is useful as an organic phosphine ligand. |
| Use | large sterically hindered phosphine ligand, it can be used for palladium-catalyzed cross-coupling reaction of aminoethyl trifluoroborate with electron-deficient aryl bromide. |