A7332312
(S)-(-)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl , 98% , 100165-88-6
Synonym(s):
(R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl;(S)-(−)-2,2′-p-tolyl-phosphino)-1,1′-binaphthyl;(S)-Tol-BINAP
CAS NO.:100165-88-6
Empirical Formula: C48 H40 P2
Molecular Weight: 678.78
MDL number: MFCD00269856
EINECS: 1312995-182-4
Pack Size | Price | Stock | Quantity |
250MG | RMB84.80 | In Stock |
|
1G | RMB306.40 | In Stock |
|
5G | RMB1450.40 | In Stock |
|
25g | RMB3199.20 | In Stock |
|
others | Enquire |
Update time: 2022-07-08
PRODUCT Properties
Melting point: | 252-256 °C |
alpha | -160° (c 0.5, C6H6) |
Boiling point: | 754.4±60.0 °C(Predicted) |
storage temp. | Inert atmosphere,Room Temperature |
form | Powder |
color | White |
optical activity | [α]20/D -156°, c = 0.5 in benzene |
Water Solubility | Insoluble in water. |
InChIKey | IOPQYDKQISFMJI-UHFFFAOYSA-N |
CAS DataBase Reference | 100165-88-6(CAS DataBase Reference) |
Description and Uses
(S)-T-BINAP reacts with silver nitrate to form (S)-Tol-BINAP·AgNO3, which can catalyze the enantioselective allylation reaction of aldehydes to form enantiopure secondary alcohols. It may be used as a chiral ligand in the palladium catalyzed asymmetric double carbohydroamination of iodoarenes to form α-aminoamides. It can also catalyze the asymmetric N-allylation reaction of ortho-tert-butylanilide derivatives with diallyl carbonate to form chiral N-allyl ortho-tert-butylanilides.
Safety
Symbol(GHS) | GHS07 |
Signal word | Warning |
Hazard statements | H315-H319-H335 |
Precautionary statements | P261-P280a-P304+P340-P305+P351+P338-P405-P501a |
Risk Statements | 36/37/38 |
Safety Statements | 26-36/37/39 |
WGK Germany | 3 |
TSCA | No |
HS Code | 29333990 |