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Molecule
ID:89009
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₀N₂O
Molecular Mass
162.1885
Exact Mass
162.07931295
Charge
0
InChI
InChI=1S/C9H10N2O/c12-8-4-2-1-3-7(8)9-10-5-6-11-9/h1-4,12H,5-6H2,(H,10,11)
InChIKey
CSFVISOIQMHABM-UHFFFAOYSA-N
Canonic Smiles
Oc1ccccc1C1=NCCN1
Isomeric Smiles
N1=C(c2ccccc2O)NCC1
Calculated Properties
JChem
Acid pKa
7.6967444
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-1.2016798
LogD (pH = 7.4)
0.22052933
Log P
0.4941984
Molar Refractivity
46.9988
Polarizability
17.57785
Polar Surface Area
44.62
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Molecular Spectra
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Data Source
Commercial Catalog
Apollo Scientific
OR4448
Sigma Aldrich
654698
Enamine
EN300-124582
Academic Data
PubChem
5354069
Names and Identifiers
IUPAC Traditional name
2-(4,5-dihydro-1H-imidazol-2-yl)phenol
Synonyms
2-(4,5-Dihydro-1H-imidazol-2-yl)phenol
o-2-Imidazolin-2-yl-phenol
2-(4,5-Dihydro-1H-imidazol-2-yl)phenol
2-(4,5-二氢-1H-咪唑-2-基)酚
2-(2-Hydroxyphenyl)-2-imidazoline
IUPAC name
2-(4,5-dihydro-1H-imidazol-2-yl)phenol
Registration numbers
MDL Number
MFCD01106478
PubChem SID
162075895
24884056
PubChem CID
5354069
CAS Number
1565-39-5
Properties
Physical Property
Melting Point
205-209 °C
Source
199 - 201°C
Source
Hydrophobicity(logP)
1.976
Source
Safety Information
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
36/37/38
Source
German water hazard class
2
Source
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
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
MSDS Link
Download link
Source
GHS Signal Word
Warning
Source
Safety Statements
26
Source
Product Information
Purity
97%
Source
95%
Source
Empirical Formula (Hill Notation)
C9H10N2O
Source
Molecule Details
Sigma Aldrich
654698
Packaging
1, 5 g in glass bottle
Application
Reactant for synthesis of:
• Polymer-anchored oxovanadium(IV) complex1
• α1-Adrenoceptor agonists2Reactant for:
• Oxidative aromatization reactions of imidazolines3
• Intramolecular nitrogen-phosphorous interactions of phosphate esters4
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay