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ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Amino alcohol derivative >  (1R,2S)-1-Amino-2-indanol

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

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

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
  • OLED
Mol File:
136030-00-7.mol
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(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
pka
14.79±0.40(Predicted)
form 
Powder
color 
White to light beige
optical activity
[α]22/D +63°, c = 0.2 in chloroform
Water Solubility 
soluble
BRN 
2803743
CAS DataBase Reference
136030-00-7(CAS DataBase Reference)
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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

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(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

Uses

This 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.

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