Substance
ID:327736
Names and Identifiers
IUPAC name
(1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol
IUPAC Traditional name
(1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol
Synonyms
(1R,2S)-(+)-cis-1-Amino-2-indanol(1R,2S)-(+)-cis-1-Amino-2-hydroxyindane(1R,2S)-(+)-顺式-1-氨基-2-茚满醇(1R,2S)-(+)-顺式-1-氨基-2-茚醇
Registration numbers
MDL Number
CAS Number
PubChem SID
Beilstein Number
Properties
Safety Information
GHS Precautionary statements
P261-P305+P351+P338
Risk Statements
36/37/38
German water hazard class
3
Safety Statements
26-36
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
European Hazard Symbols
Irritant (Xi)MSDS Link
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Signal Word
Warning
GHS Hazard statements
H315-H319-H335
Physical Property
Optical Rotation
[α]22/D +63°, c = 0.2 in chloroform
Melting Point
118-121 °C(lit.)
Product Information
Purity
99%
Empirical Formula (Hill Notation)
C9H11NO
Optical Purity
ee: 99% (GLC)
Molecule Details
Packaging
1, 5 g in glass bottle
Application
This cis-aminoindanol and its antipode have been used in the preparation of a series of potent HIV-1 protease inhibitory peptides.1,2,3,4,5,6,7,8 Also, they have served as chiral ligands in the catalytic asymmetric reduction of prochiral ketones with boranes.9,10
1, 5 g in glass bottle
Application
This cis-aminoindanol and its antipode have been used in the preparation of a series of potent HIV-1 protease inhibitory peptides.1,2,3,4,5,6,7,8 Also, they have served as chiral ligands in the catalytic asymmetric reduction of prochiral ketones with boranes.9,10
Molecular Spectra
No Data Available
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References
No Data Available
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