163061-73-2
Chemical Structure
(1R,2R)-1-Aminoindan-2-ol
- CAS No.: 163061-73-2
- Formula:C9H11NO
- Molecular Weight:149.19
IUPAC Name: (1R,2R)-1-amino-2,3-dihydro-1H-inden-2-ol
InChIKey: LOPKSXMQWBYUOI-RKDXNWHRSA-N
SMILES: O[C@H]1[C@@H](C2=C(C1)C=CC=C2)N
Biological Activity: (1R,2R)-1-Aminoindan-2-ol is the isomer of (1S,2R)-1-Aminoindan-2-ol (HY-W002530), and can be used as a biological material or organic compound for life science related research. (1R,2R)-1-Aminoindan-2-ol can be used as a starting material to prepare an indene-based chiral auxiliary that is used in the aldol reaction. (1R,2R)-1-Aminoindan-2-ol can be used as a starting material in the synthesis of oxazoline-alcohol ligands[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
(1R,2R)-1-Aminoindan-2-ol | 99.70% | (1R,2R)-1-Aminoindan-2-ol is the isomer of (1S,2R)-1-Aminoindan-2-ol (HY-W002530), and can be used as a biological material or organic compound for life science related research. (1R,2R)-1-Aminoindan-2-ol can be used as a starting material to prepare an indene-based chiral auxiliary that is used in the aldol reaction. (1R,2R)-1-Aminoindan-2-ol can be used as a starting material in the synthesis of oxazoline-alcohol ligands. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017;16(5):315-337. [Content Brief]
- [2]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-985. [Content Brief]
- [3]. Osorio-Lozada, A., & Olivo, H. F. (2008). Indene-based thiazolidinethione chiral auxiliary for propionate and acetate aldol additions. Organic letters, 10(4), 617–620. [Content Brief]
- [4]. Timothy Noël, et al., Efficient one-step synthesis of chiral bidentate oxazoline-alcohol ligands via a cyclic imidate ester rearrangement, Tetrahedron: Asymmetry, Volume 20, Issue 17, 2009, Pages 1962-1968, ISSN 0957-4166.
