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Molecule
ID:31191
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₂₀N₂O
Molecular Mass
220.3107
Exact Mass
220.15756327
Charge
0
InChI
InChI=1S/C13H20N2O/c14-12-4-6-13(7-5-12)16-11-10-15-8-2-1-3-9-15/h4-7H,1-3,8-11,14H2
InChIKey
VTBHKDHFDNLZNG-UHFFFAOYSA-N
Canonic Smiles
Nc1ccc(cc1)OCCN1CCCCC1
Isomeric Smiles
N1(CCOc2ccc(N)cc2)CCCCC1
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.4004567
LogD (pH = 7.4)
0.27520216
Log P
1.8556592
Molar Refractivity
67.3827
Polarizability
25.841887
Polar Surface Area
38.49
Rotatable Bonds
4
Lipinski's Rule of Five
true
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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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IUPAC Traditional name
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IUPAC name
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MDL Number
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PubChem SID
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PubChem CID
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
033867
Life Chemicals
F2169-0796
Enamine
EN300-112257
Academic Data
PubChem
3016025
Names and Identifiers
IUPAC Traditional name
4-[2-(piperidin-1-yl)ethoxy]aniline
Synonyms
4-(2-Piperidin-1-yl-ethoxy)-phenylamine
4-[2-(piperidin-1-yl)ethoxy]aniline
IUPAC name
4-[2-(piperidin-1-yl)ethoxy]aniline
Registration numbers
MDL Number
MFCD07365100
PubChem SID
160994498
PubChem CID
3016025
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Product Information
Purity
95+%
Source
95%
Source
Physical Property
Partition Coefficient
2.041
Source
Hydrophobicity(logP)
2.337
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay