| Weight | 149.193 g/mol |
|---|---|
| Formula | C9H11NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
1-Amino-2-indanol (74165-73-4)
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- 1R,2S)-(+)-cis-1-amino-2-indanol: An effective ligand for asymmetric catalysis of transfer hydrogenations of ketones. (Journal of Organic Chemistry, 1997)
- Amino-indanol-catalyzed asymmetric Michael additions of oxindoles to protected 2-amino-1-nitroethenes for the synthesis of 3,3'-disubstituted oxindoles bearing ,-diamino functionality. (Journal of Organic Chemistry, 2011)
- cis-1-amino-2-indanol in asymmetric synthesis. Part I. A practical catalyst system for the enantioselective borane reduction of aromatic ketones (Tetrahedron Letters, 1994)
- cis-1-Amino-2-indanol in Drug Design and Applications to Asymmetric Processes (Chemical Reviews, 2006)
- An efficient phosphorus-containing oxazoline ligand derived from cis-2-amino-3,3-dimethyl-1-indanol: application to the palladium-catalyzed asymmetric Heck reaction (Tetrahedron-asymmetry, 2000)
- Synthesis of enantiomerically pure trans-(1R,2R)- and cis-(1S,2R)-1-amino-2-indanol by lipase and -transaminase (Biotechnology and Bioengineering, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(C(C2=CC=CC=C21)N)O
-
InChIKeyLOPKSXMQWBYUOI-UHFFFAOYSA-N
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Synthesis
Reactant
+
BENZYL CHLORIDE
(Grignard alcohol)
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