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6351-10-6 molecular structure
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(1S)-2,3-dihydro-1H-inden-1-ol

ChemBase ID: 111946
Molecular Formular: C9H10O
Molecular Mass: 134.1751
Monoisotopic Mass: 134.07316494
SMILES and InChIs

SMILES:
O[C@H]1CCc2ccccc12
Canonical SMILES:
O[C@H]1CCc2c1cccc2
InChI:
InChI=1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2/t9-/m0/s1
InChIKey:
YIAPLDFPUUJILH-VIFPVBQESA-N

Cite this record

CBID:111946 http://www.chembase.cn/molecule-111946.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(1S)-2,3-dihydro-1H-inden-1-ol
IUPAC Traditional name
(1S)-2,3-dihydro-1H-inden-1-ol
Synonyms
(S)-(+)-1-Hydroxyindan
(S)-(+)-1-Indanol
L-INDANOL
(1S)-2,3-dihydro-1H-inden-1-ol
(S)-(+)-1-羟基茚满
(S)-(+)-1-茚醇
CAS Number
6351-10-6
25501-32-0
MDL Number
MFCD00064165
Beilstein Number
2206709
PubChem SID
24859215
162096756
PubChem CID
6971242

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 14.475292  H Acceptors
H Donor LogD (pH = 5.5) 1.7501203 
LogD (pH = 7.4) 1.7501203  Log P 1.7501203 
Molar Refractivity 40.4547 cm3 Polarizability 15.667024 Å3
Polar Surface Area 20.23 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Pharmacology Properties Product Information Bioassay(PubChem)
Melting Point
69-73 °C expand Show data source
69-73 °C(lit.) expand Show data source
Optical Rotation
[α]20/D +30°, c = 2 in chloroform expand Show data source
[α]20/D +31±2°, c = 1% in chloroform expand Show data source
Hydrophobicity(logP)
1.518 expand Show data source
European Hazard Symbols
Harmful Harmful (Xn) 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
22-36/37/38 expand Show data source
Safety Statements
26-36 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H302-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
Storage Temperature
2-8°C expand Show data source
Gene Information
human ... UGT2B17(7367), UGT2B7(7364) expand Show data source
Purity
≥99.0% (sum of enantiomers, GC) expand Show data source
95% expand Show data source
99% expand Show data source
Grade
puriss. expand Show data source
Optical Purity
enantiomeric ratio: ≥98:2 (NMR) expand Show data source
Certificate of Analysis
Download expand Show data source
Empirical Formula (Hill Notation)
C9H10O expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich
MP Biomedicals - 05221903 external link
MP Biomedicals Rare Chemical collection
Sigma Aldrich - 323128 external link
Packaging
1, 5 g in glass bottle

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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