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
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
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
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
BOX ligand complex enhances catalytic enantioselective aziridination of styrene, with phenyl substituents proving superior over t-Bu groups.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service