CAS 136030-00-7
:(+)-cis-1-Amino-2-indanol
Description:
(+)-cis-1-Amino-2-indanol is an organic compound characterized by its chiral structure, which includes an amino group and an indanol moiety. This compound is a derivative of indole, featuring a hydroxyl group attached to a carbon adjacent to the amino group, contributing to its unique properties. The cis configuration indicates that the amino and hydroxyl groups are on the same side of the indanol ring, influencing its stereochemistry and reactivity. This compound is often studied for its potential applications in pharmaceuticals and as a chiral building block in organic synthesis. Its ability to form hydrogen bonds due to the presence of the amino and hydroxyl groups enhances its solubility in polar solvents. Additionally, the presence of the indanol structure may impart interesting biological activities, making it a subject of interest in medicinal chemistry. Overall, (+)-cis-1-amino-2-indanol is notable for its chiral nature, functional groups, and potential utility in various chemical applications.
Formula:C9H11NO
InChI: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+/m0/s1
InChI key:InChIKey=LOPKSXMQWBYUOI-DTWKUNHWSA-N
SMILES:N[C@@H]1C=2C(C[C@@H]1O)=CC=CC2
Synonyms:- ((1R,2S)-2-Hydroxyindan-1-yl)amine
- (+)-cis-1-Amino-2-indanol
- (1R,2S)-(+)-1-Amino-2-Hydroxyindan
- (1R,2S)-(+)-CIS-1-Amino-2-Hydroxyindane
- (1R,2S)-(-)-cis-1-aminoindan-2-ol
- (1R,2S)-1-Amino-1H-Indan-2-OL
- (1R,2S)-1-Amino-Indan-2-OL
- (1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol
- (1R,2S)-2,3-Dihydro-2-hydroxyinden-1-ylamine
- (1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-aminium
- (1R,2S)-Cis-1-Amino-2-indanol
- 1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1R,2S)-
- 1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1R-cis)-
- CIS-(1R, 2S)-1-Amino-2-Indanol
- See more synonyms
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Found 6 products.
(1R,2S)-(+)-1-Amino-2-indanol
CAS:Formula:C9H11NOPurity:>98.0%(GC)(T)Color and Shape:White to Orange to Green powder to crystalMolecular weight:149.19(+)-cis-1-Amino-2-indanol
CAS:Formula:C9H11NOPurity:98%Color and Shape:SolidMolecular weight:149.1897(1R,2S)-1-Amino-2-hydroxyindane
CAS:<p>(1R,2S)-1-Amino-2-hydroxyindane</p>Formula:C9H11NOPurity:98%Color and Shape: white to off-white solidMolecular weight:149.19g/mol(1R,2S)-1-Amino-2-indanol
CAS:<p>(1R,2S)-1-Amino-2-indanol is a potential drug candidate that can be used in asymmetric synthesis. It has been shown to inhibit the flow of hydrogen bond and to form an enantiomer. The enantiomer is more active than the racemic mixture, which may be due to the higher binding affinity for the enzyme. This compound has also been shown to inhibit herpes simplex virus and HIV in vitro with a high potency. (1R,2S)-1-Amino-2-indanol is modeled using molecular dynamics simulations and quantum mechanical calculations.</p>Purity:Min. 95%Color and Shape:PowderMolecular weight:149.19 g/mol(1R,2S)-(+)-cis-1-Amino-2-indanol
CAS:Formula:C9H11NOPurity:98%Color and Shape:SolidMolecular weight:149.193(1R,2S)-(+)-cis-1-Aminoindan-2-ol, 98%
CAS:<p>(1R,2S)-(+)-cis-1-Aminoindan-2-ol, 98%</p>Formula:C9H11NOPurity:98%Color and Shape:white to off-white pwdr.Molecular weight:149.19





