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136030-00-7 molecular structure
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(1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol

ChemBase ID: 67670
Molecular Formular: C9H11NO
Molecular Mass: 149.18974
Monoisotopic Mass: 149.08406398
SMILES and InChIs

SMILES:
[C@@H]1([C@H](Cc2ccccc12)O)N
Canonical SMILES:
N[C@H]1[C@@H](O)Cc2c1cccc2
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
InChIKey:
LOPKSXMQWBYUOI-DTWKUNHWSA-N

Cite this record

CBID:67670 http://www.chembase.cn/molecule-67670.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
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-hydroxyindane
(1R,2S)-(+)-cis-1-Amino-2-indanol
(1R,2S)-1-Amino-2-indanol
(1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol
(1R,2S)-(+)-顺式-1-氨基-2-茚满醇
(1R,2S)-(+)-顺式-1-氨基-2-茚醇
CAS Number
136030-00-7
MDL Number
MFCD00216656
Beilstein Number
2803743
PubChem SID
162033405
24846036
24867628
PubChem CID
2725045

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 14.380486  H Acceptors
H Donor LogD (pH = 5.5) -2.3743553 
LogD (pH = 7.4) -1.1841465  Log P 0.5683349 
Molar Refractivity 43.4737 cm3 Polarizability 17.190062 Å3
Polar Surface Area 46.25 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
118-121 °C(lit.) expand Show data source
Optical Rotation
[α]20/D +63±5°, c = 0.2% in chloroform expand Show data source
[α]22/D +63°, c = 0.2 in chloroform expand Show data source
Hydrophobicity(logP)
0.348 expand Show data source
Storage Warning
IRRITANT expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
36/37/38 expand Show data source
Safety Statements
26-36 expand Show data source
TSCA Listed
false expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Purity
≥99.0% (sum of enantiomers, GC) expand Show data source
95% expand Show data source
95+% expand Show data source
99% expand Show data source
Grade
purum expand Show data source
Optical Purity
ee: 99% (GLC) expand Show data source
Empirical Formula (Hill Notation)
C9H11NO expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 440841 external link
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

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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