A7332412
(S)-(-)-XylBINAP , 97% , 135139-00-3
Synonym(s):
(S)-(−)-2,2′-Bis[bis(3,5-dimethylphenyl)phosphino]-1,1′-binaphthyl;(S)-(−)-2,2′-Bis[di(3,5-xylyl)phoshino]-1,1′-binaphthyl;(S)-3,5-Xylyl-BINAP
CAS NO.:135139-00-3
Empirical Formula: C52H48P2
Molecular Weight: 734.89
MDL number: MFCD01630821
EINECS: 681-146-8
Pack Size | Price | Stock | Quantity |
100MG | RMB93.60 | In Stock |
|
200mg | RMB167.20 | In Stock |
|
500MG | RMB375.20 | In Stock |
|
1g | RMB454.40 | In Stock |
|
5g | RMB1758.40 | In Stock |
|
others | Enquire |
Update time: 2022-07-08
PRODUCT Properties
Melting point: | 203-206°C |
alpha | -172 º (c=1 in chloroform) |
Boiling point: | 825.3±65.0 °C(Predicted) |
storage temp. | Inert atmosphere,Room Temperature |
Water Solubility | Insoluble in water |
form | crystal |
color | white to pale yellow |
Description and Uses
Catalyst for:
- Asymmetric hydrogenation of benzophenone
- Regio- and stereoselective preparation of axially chiral arylnaphthalene derivatives via rhodium-catalyzed [2+2+2] cycloaddition of diynes with naphthalenepropynoic acid derivatives in the presence of chiral biaryl bisphosphine ligands
- Regiodivergent rhodium-catalyzed [(2+2)+2] carbocyclization of 1,6-enynes with Me propiolates
- Ligand controlled regioselective and stereoselective desymmetrizing rhodium-catalyzed allylic arylation of meso cyclopentene dicarbonates with arylboronic acids to form regioisomeric arylcyclopentenols
- Platinum(II) complex-catalyzed enantioselective aldol reaction with ketene silyl acetals in DMF at room temperature
- Stereoselective preparation of chiral N,O-biaryls via Rh-catalyzed [2+2+2] cycloaddition of conjugate ynamides with diynes
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 | 26-37 |
TSCA | No |
HS Code | 2931.90.6000 |