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Molecule
ID:20124
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₃NO₂
Molecular Mass
215.24782
Exact Mass
215.09462866
Charge
0
InChI
InChI=1S/C13H13NO2/c1-15-12-4-2-3-5-13(12)16-11-8-6-10(14)7-9-11/h2-9H,14H2,1H3
InChIKey
XFOFRBMGVDBINH-UHFFFAOYSA-N
Canonic Smiles
COc1ccccc1Oc1ccc(cc1)N
Isomeric Smiles
c1(Oc2ccc(N)cc2)c(OC)cccc1
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
2.4634676
LogD (pH = 7.4)
2.486632
Log P
2.4869359
Molar Refractivity
63.4624
Polarizability
24.31769
Polar Surface Area
44.48
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
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Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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PubChem SID
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PubChem CID
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MDL Number
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CAS Number
Properties
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Safety Information
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4008766
Apollo Scientific
OR11344
InterBioScreen
BB_SC-8273
Matrix Scientific
022435
Enamine
EN300-23796
Alfa Aesar
H32565
Academic Data
PubChem
1121067
Names and Identifiers
IUPAC name
4-(2-methoxyphenoxy)aniline
Synonyms
4-(2-Methoxyphenoxy)aniline
4-(2-Methoxyphenoxy)aniline
4-(2-甲氧基苯氧基)苯胺
IUPAC Traditional name
4-(2-methoxyphenoxy)aniline
Registration numbers
PubChem SID
160983431
PubChem CID
1121067
MDL Number
MFCD02663341
CAS Number
13066-01-8
Properties
Safety Information
MSDS Link
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Irritant
Source
GHS Precautionary statements
P261
-
P301+P310
-
P305+P351+P338
-
P302+P352
-
P405
-P501A
Source
GHS Hazard statements
H301
-
H315
-
H319
-
H335
Source
Safety Statements
26
-
36/37
Source
Risk Statements
22
-
36/37/38
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
European Hazard Symbols
Harmful (X)
Source
Physical Property
Melting Point
92.2-94.4°C
Source
Hydrophobicity(logP)
2.582
Source
Product Information
Purity
95%
Source
97%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay