495301
(+)-2,2′-Isopropylidenebis[(4R)-4-benzyl-2-oxazoline]
98%
Synonym(s):
(R,R)-(+)-2,2′-Isopropylidenebis(4-benzyl-2-oxazoline), [R(R*,R*)]-(+)-2,2′-Isopropylidenebis(4-benzyl-2-oxazoline)
About This Item
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Assay
98%
optical activity
[α]22/D +65°, c = 1 in ethanol
mp
54-60 °C (lit.)
functional group
ether
phenyl
storage temp.
2-8°C
SMILES string
CC(C)(C1=N[C@@H](CO1)Cc2ccccc2)C3=N[C@@H](CO3)Cc4ccccc4
InChI
1S/C23H26N2O2/c1-23(2,21-24-19(15-26-21)13-17-9-5-3-6-10-17)22-25-20(16-27-22)14-18-11-7-4-8-12-18/h3-12,19-20H,13-16H2,1-2H3/t19-,20-/m1/s1
InChI key
GAKCKAKYRQUVRK-WOJBJXKFSA-N
related product
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
BOX ligand complex enhances catalytic enantioselective aziridination of styrene, with phenyl substituents proving superior over t-Bu groups.
BOX ligand complex enhances catalytic enantioselective aziridination of styrene, with phenyl substituents proving superior over t-Bu groups.
BOX ligand complex enhances catalytic enantioselective aziridination of styrene, with phenyl substituents proving superior over t-Bu groups.
BOX ligand complex enhances catalytic enantioselective aziridination of styrene, with phenyl substituents proving superior over t-Bu groups.
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