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About This Item
Empirical Formula (Hill Notation):
C18H28N2P2
CAS Number:
Molecular Weight:
334.38
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
≥95%
form
solid
mp
100-104 °C
functional group
phosphine
SMILES string
CP(c1nc2ccccc2nc1P(C)C(C)(C)C)C(C)(C)C
InChI
1S/C18H28N2P2/c1-17(2,3)21(7)15-16(22(8)18(4,5)6)20-14-12-10-9-11-13(14)19-15/h9-12H,1-8H3/t21-,22-/m0/s1
InChI key
DRZBLHZZDMCPGX-VXKWHMMOSA-N
Related Categories
General description
(R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline is an air-stable C2-symmetric P-stereogenic phosphine ligand.
Application
Efficient ligand exhibiting high levels of enantiocontrol in synthetic transformations ranging from metal-catalyzed 1,4-addition of arylboronic acids to alkylative ring opening to asymmetric hydrogenation.
Features and Benefits
Advantages of the QuinoxP* Ligands:
- It is not oxidized nor epimerized at ambient conditions in air
- Enantioselectivities are outstanding for various reaction paradigms
- Hydrogenations proceed under mild reaction conditions
- Low catalyst loadings yield high TONs
Legal Information
QuinoxP is a registered trademark of Nippon Chemical Industry Co., Ltd.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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