405973
2,2′-Bis[(4S)-4-benzyl-2-oxazoline]
98%
Synonym(s):
(S,S)-4,4′-Dibenzyl-2,2′-bi(2-oxazoline), (S,S)-2,2′-Bis(4-benzyl-2-oxazoline)
About This Item
Recommended Products
Quality Level
Assay
98%
form
solid
optical activity
[α]20/D −40.6°, c = 1 in ethanol
mp
129-132 °C (lit.)
SMILES string
C1OC(=N[C@H]1Cc2ccccc2)C3=N[C@H](CO3)Cc4ccccc4
InChI
1S/C20H20N2O2/c1-3-7-15(8-4-1)11-17-13-23-19(21-17)20-22-18(14-24-20)12-16-9-5-2-6-10-16/h1-10,17-18H,11-14H2/t17-,18-/m0/s1
InChI key
OIEQQWQZUYZCRJ-ROUUACIJSA-N
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Application
- A catalyst for the enantioselective hydrosilylation of ketones.
- A Schiff base ligand in the preparation of rhodium(I) and palladium(II) coordination complexes.
- A ligand in the formation of copper(I) halide complexes; applicable in the synthesis of coordination polymers.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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Articles
C2-symmetric chiral bisoxazolines (BOX) are privileged structures because they promote a great number of transformations with unprecedented selectivity.1
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