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(1R,2S)-1-Amino-2-indanol

CAS# 136030-00-7

(1R,2S)-1-Amino-2-indanol

Catalog No. BCC8381----Order now to get a substantial discount!

Product Name & Size Price Stock
(1R,2S)-1-Amino-2-indanol: 5mg $17 In Stock
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Chemical structure

(1R,2S)-1-Amino-2-indanol

3D structure

Chemical Properties of (1R,2S)-1-Amino-2-indanol

Cas No. 136030-00-7 SDF Download SDF
PubChem ID 2725045 Appearance Powder
Formula C9H11NO M.Wt 149
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol
SMILES C1C(C(C2=CC=CC=C21)N)O
Standard InChIKey LOPKSXMQWBYUOI-DTWKUNHWSA-N
Standard 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
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

(1R,2S)-1-Amino-2-indanol Dilution Calculator

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(1R,2S)-1-Amino-2-indanol Molarity Calculator

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Preparing Stock Solutions of (1R,2S)-1-Amino-2-indanol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.7114 mL 33.557 mL 67.1141 mL 134.2282 mL 167.7852 mL
5 mM 1.3423 mL 6.7114 mL 13.4228 mL 26.8456 mL 33.557 mL
10 mM 0.6711 mL 3.3557 mL 6.7114 mL 13.4228 mL 16.7785 mL
50 mM 0.1342 mL 0.6711 mL 1.3423 mL 2.6846 mL 3.3557 mL
100 mM 0.0671 mL 0.3356 mL 0.6711 mL 1.3423 mL 1.6779 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on (1R,2S)-1-Amino-2-indanol

A photo-responsive macroscopic switch constructed using a chiral azo-calix[4]arene functionalized silicon surface.[Pubmed:29504616]

Chem Commun (Camb). 2018 Mar 25;54(24):2978-2981.

A photo-responsive macroscopic switch was fabricated using a chiral azo-calix[4]arene derivative (FC4AD) functionalized silicon surface and exhibited selective and reversible recognition of (1R,2S)-1-Amino-2-indanol through the variation of wettability. This photo-responsive device may have wide applications in controlled release of chiral drugs and in biosensors.

Cyclohydrocarbonylation-based strategy toward poly-substituted piperidines.[Pubmed:21462951]

Org Lett. 2011 May 6;13(9):2294-7.

Convenient accesses to enantiomerically pure 2-, 2,3-, 2,6-, 2,3,6-substituted piperidines and 1,4-substituted indolizine are described. At first, indium-mediated aminoallylation and -crotylation of aldehydes with (R)-phenylglycinol or (1R,2S)-1-Amino-2-indanol gave homoallylamines with high stereocontrol. Then, these products, submitted to a Rh(I)-catalyzed hydroformylative cyclohydrocarbonylation, afforded perhydrooxazolo[3,2-a]piridines whose oxazolidines are opened with nucleophiles. Finally, the removal of the chiral auxiliaries delivered the enantiomerically pure piperidines.

Synthesis of enantiopure oxorhenium(V) and arylimidorhenium(V) "3 + 2" Schiff base complexes. X-ray diffraction, cyclic voltammetry, UV-vis, and circular dichroism characterizations.[Pubmed:11735489]

Inorg Chem. 2001 Dec 17;40(26):6767-73.

Two new oxorhenium(V) and two new arylimidorhenium(V) complexes of the Schiff base ligands 2-hydroxybenzaldehyde-((1R,2S)-1-Amino-2-indanol)imine (1) (H(2)L(1)) and 3-(1-adamantyl)-2-hydroxy-5-methylbenzaldehyde-((1R,2S)-1-amino- 2-indanol)imine (2) (H(2)L(2)) have been prepared from the reaction of the precursor Re(O)(PPh(3))(2)Cl(3), Re(NC(6)H(5))(PPh(3))(2)Cl(3), or Re(NC(6)H(4)OCH(3))(PPh(3))(2)Cl(3) and the free ligands H(2)L(1,2). The complexes Re(O)(HL(1))(L(1)) (3), Re(O)(HL(2))(L(2)) (4), Re(NC(6)H(5))(HL(1))(L(1)) (5), and Re(NC(6)H(4)OCH(3))(HL(1))(L(1)) (6) have been isolated and fully characterized by IR, (1)H NMR, circular dichroism, LRMS-FAB, and elemental analysis. All the complexes have a chiral center at rhenium. A single enantiomer is obtained in all cases. Suitable crystals of 3 and 5 were used in X-ray structural determinations. Crystal data: (3) C(32)H(27)N(2)O(5)Re.CH(2)Cl(2), orthorhombic, P2(1)2(1)2(1), a = 9.5599(16) A, b = 9.9579(16) A, c = 31.712(5) A, V = 3018.9(9) A(3), T = 100(2) K, Z = 4. (5) C(40)H(38)N(3)O(5)Re, monoclinic, P2(1), a = 9.286(3) A, b = 18.759(6) A, c = 9.957(3) A, beta = 102.817(6) degrees, V = 1691.3(10) A(3), T = 100(2) K, Z = 2. The major characteristic of these complexes is the presence of two coordination modes for the Schiff base ligands on rhenium, a tridentate ligand (noted L(1,2)) and another bidentate ligand (noted HL(1,2)). In the latter, the -OH group of the indanol is free and tilts away from the coordination sphere. X-ray structural analyses in conjunction with circular dichroism were used to assign the absolute configuration at rhenium (C). Cyclic voltammetry, UV-vis, and circular dichroism data are presented and discussed. The complexes were found to be highly stable and to resist reduction even when treated with organic phosphanes.

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