Name | R-(-)-1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate |
Synonyms | (R)-(-)-1,1'-Biphthyl-2,2'-diyl hydrogenphosphate R-(-)-1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate (R)-(-)-1,1'-Binaphthyl-2,2'-diylhydrogenphosphate (R)-(-)-1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate (R)-(-)-1,1'-Binaphthyl-2,2'-diyl hydrogen phosphate (R)-(-)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGEN PHOSPHONATE (R)-(-)-1,1'-Binaphthalene-2,2'-diyl hydrogen phosphate (R)-(-)-1,1'-Binaphthyl-2,2'-diyl Hydrogen Phosphate, (R)-(-)-BNDHP (R)-5,5',6,6',7,7',8,8'-Octahydro-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate |
CAS | 39648-67-4 |
EINECS | 609-734-1 |
InChI | InChI=1/C20H13O4P/c21-25(22)23-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)24-25/h1-12H,(H,21,22)/p-1 |
Molecular Formula | C20H13O4P |
Molar Mass | 348.29 |
Density | 1.49±0.1 g/cm3(Predicted) |
Melting Point | ≥300°C |
Boling Point | 619.5±38.0 °C(Predicted) |
Specific Rotation(α) | -607.5 º (c=1.4,MeOH) |
Flash Point | 328.5°C |
Solubility | Solubility in hot Methanol, almost transparency. |
Vapor Presure | 3.3E-16mmHg at 25°C |
Appearance | White-like powder |
Color | white |
BRN | 4713363 |
pKa | 1.14±0.20(Predicted) |
Storage Condition | Inert atmosphere,Room Temperature |
Refractive Index | -595 ° (C=1, MeOH) |
MDL | MFCD00010045 |
Physical and Chemical Properties | Melting point 300 °c. |
Use | As a chiral ligand in hydrocarboxylation reaction; In isomer-selective mannich reaction, it is used as a chiral bronsted acid catalyst. |
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 - Wear suitable protective clothing. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S22 - Do not breathe dust. |
UN IDs | 3464 |
WGK Germany | 3 |
RTECS | RZ2475100 |
FLUKA BRAND F CODES | 10-23 |
HS Code | 29199000 |
Use | Chiral ligand for hydrocarboxylation reaction; used for asymmetric Mannich reaction catalyzed by chiral Bronsted acid; used for asymmetric dipolar cycloaddition reaction with rhodium complexation and regulation of diazo compounds; used for racemic amines that are difficult to separate; palladium derivatives have been used for asymmetric hydrocarboxylation reactions, and rhodium derivatives have been used in dipolar cycloaddition reactions |