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Assay
97%
form
solid
optical activity
[α]/D -23.0°, c = 1 in ethanol
mp
142-146 °C
functional group
hydroxyl
SMILES string
N[C@H]1[C@H](O)Cc2ccccc12
InChI
1S/C9H11NO/c10-9-7-4-2-1-3-6(7)5-8(9)11/h1-4,8-9,11H,5,10H2/t8-,9-/m1/s1
InChI key
LOPKSXMQWBYUOI-RKDXNWHRSA-N
Application
(1R,2R)-(−)-trans-1-Amino-2-indanol has been used as a starting material to prepare an indene-based chiral auxiliary, which is used in the aldol reaction.
It can also be used as:
It can also be used as:
- A starting material in the synthesis of oxazoline-alcohol ligands, which are employed in the asymmetric addition reaction of diethylzinc to aldehydes.
- A chiral test compound in the study of enantiomeric separation of chiral primary amines using supercritical fluid chromatography (SFC) and HPLC.
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
dust mask type N95 (US), Eyeshields, Gloves
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Indene-based thiazolidinethione chiral auxiliary for propionate and acetate aldol additions
Organic Letters, 10(4), 617-620 (2008)
Efficient one-step synthesis of chiral bidentate oxazoline-alcohol ligands via a cyclic imidate ester rearrangement
Tetrahedron Asymmetry, 20(17), 1962-1968 (2009)
Comparison of enantiomeric separations and screening protocols for chiral primary amines by SFC and HPLC
LCGC North America, 32(17), 742-752 (2014)
Chromatograms
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