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Molecule
ID:16170
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₃NO
Molecular Mass
199.24842
Exact Mass
199.09971404
Charge
0
InChI
InChI=1S/C13H13NO/c14-12-7-4-8-13(9-12)15-10-11-5-2-1-3-6-11/h1-9H,10,14H2
InChIKey
IGPFOKFDBICQMC-UHFFFAOYSA-N
Canonic Smiles
Nc1cccc(c1)OCc1ccccc1
Isomeric Smiles
c1c(OCc2ccccc2)cccc1N
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
2.6983197
LogD (pH = 7.4)
2.7109582
Log P
2.7111218
Molar Refractivity
61.8342
Polarizability
23.606153
Polar Surface Area
35.25
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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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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Synonyms
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IUPAC name
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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
Matrix Scientific
017113
Apollo Scientific
OR8289
Sigma Aldrich
100803
Enamine
EN300-52995
Bide Pharmatech
BD84731
Academic Data
PubChem
92892
Names and Identifiers
IUPAC Traditional name
3-(benzyloxy)aniline
Synonyms
3-(Benzyloxy)aniline
3-Amino-alpha-phenylanisole
3-Benzyloxyaniline
3-苄氧基苯胺
3-Benzyloxyaniline
IUPAC name
3-(benzyloxy)aniline
Registration numbers
CAS Number
1484-26-0
MDL Number
MFCD00007784
PubChem SID
160979477
24846422
PubChem CID
92892
EC Number
216-056-6
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Harmful/Irritant
Source
MSDS Link
Download link
Source
Download link
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
German water hazard class
3
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 Hazard statements
H315
-
H319
-
H335
Source
Risk Statements
36/37/38
Source
Safety Statements
26
-
36
Source
GHS Signal Word
Warning
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
European Hazard Symbols
Irritant (Xi)
Source
Product Information
Purity
97%
Source
98%
Source
95%
Source
Linear Formula
C6H5CH2OC6H4NH2
Source
Physical Property
Melting Point
63-67°C
Source
63-67 °C(lit.)
Source
61 - 63°C
Source
Hydrophobicity(logP)
2.772
Source
Molecule Details
Sigma Aldrich
100803
Packaging
5, 10 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
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CAS Number
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EC Number