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

(1R,2S)-1-Amino-2-indanol
  • CAS No.:136030-00-7
Other grades of this product :
(1R,2S)-1-Amino-2-indanol Basic information
Uses
Product Name:(1R,2S)-1-Amino-2-indanol
Synonyms:(1R,2S)-(+)-cis-1-Amino-2-indanol,98%;1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1R,2S)-;(1R,2S)-(+)-cis-1-Amino-2-indanol ,99%;(1R,2S)-1-Aminoindan-2-ol, (1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol;(1R,2S)-(+)-cis-1-AMino-2-indanol, 98% 1GR;2S)-1-AMino-2-indanol;(1R,2S)-1-Aminoindan-2-ol, (1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol, (1R,2S)-2-Hydroxyindan-1-amine;(1R,2S)-(+)-cis-1-AMino-2-indanol 99%
CAS:136030-00-7
MF:C9H11NO
MW:149.19
EINECS:603-940-5
Product Categories:CHIRAL COMPOUNDS;organic alcohol;Amino Alcohols (Chiral);Chiral Building Blocks;Synthetic Organic Chemistry;CHIRAL CHEMICALS;chiral;API intermediates;Chiral Nitrogen
Mol File:136030-00-7.mol
(1R,2S)-1-Amino-2-indanol Chemical Properties
Melting point 118-121 °C(lit.)
alpha 44.5 º (c=1, methanol)
Boiling point 270.27°C (rough estimate)
density 1.0753 (rough estimate)
refractive index 43 ° (C=1, MeOH)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Methanol
form Powder
pka14.79±0.40(Predicted)
color White to light beige
optical activity[α]22/D +63°, c = 0.2 in chloroform
Water Solubility soluble
BRN 2803743
CAS DataBase Reference136030-00-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 26-36-36/37/39
RIDADR 2811
WGK Germany 3
10-23
TSCA No
HS Code 29061990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
(1R,2S)-1-Amino-2-indanol Usage And Synthesis
Uses(1R,2S)-1-Amino-2-indanol  Class of catalytic ligands which when used with a reducing agent, exhibit enantioselectivity in the reduction of a wide range of substrates.
Chemical Properties(1R,2S)-1-Amino-2-indanol is white to light yellow crystal powder
UsesThis cis-aminoindanol and its antipode have been used in the preparation of a series of potent HIV-1 protease inhibitory peptides. Also, they have served as chiral ligands in the catalytic asymmetric reduction of prochiral ketones with boranes.
(1R,2S)-1-Amino-2-indanol Preparation Products And Raw materials

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