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Molecule
ID:83323
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₀O₂
Molecular Mass
186.2066
Exact Mass
186.06807956
Charge
0
InChI
InChI=1S/C12H10O2/c13-10-5-4-8-12(9-10)14-11-6-2-1-3-7-11/h1-9,13H
InChIKey
HBUCPZGYBSEEHF-UHFFFAOYSA-N
Canonic Smiles
Oc1cccc(c1)Oc1ccccc1
Isomeric Smiles
O(c1cc(ccc1)O)c1ccccc1
Calculated Properties
JChem
LogD (pH = 7.4)
3.16
LogD (pH = 5.5)
3.17
Log P
3.17
Rotatable Bonds
2
H Donor
1
H Acceptors
1
Lipinski's Rule of Five
true
Acid pKa
9.10
Polar Surface Area
29.46
Polarizability
19.27
Molar Refractivity
54.28
LOG S
-3.02
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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Synonyms
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IUPAC name
Registration numbers
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
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PDB Bank
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR2613
MP Biomedicals
05205001
Sigma Aldrich
269980
Enamine
EN300-18763
Alfa Aesar
A17865
Academic Data
PubChem
12842
ChEBI
CHEBI:39263
Names and Identifiers
IUPAC Traditional name
3-phenoxyphenol
Synonyms
3-Phenoxyphenol
3-Phenoxyphenol
3-苯氧基苯酚
M-PHENOXYPHENOL
3-Hydroxyphenyl phenyl ether
3-Hydroxydiphenyl ether
3-hydroxydiphenyl ether
3-phenoxyphenol
m-phenoxyphenol
IUPAC name
3-phenoxyphenol
Registration numbers
PubChem SID
162070442
24856184
26675782
PubChem CID
12842
MDL Number
MFCD00003543
CAS Number
713-68-8
EC Number
211-930-3
CHEMBL
CHEMBL2163966
SureChEMBL Database
SCHEMBL450261
Protein Data Bank
6xq6
6xq8
Beilstein Number
1869624
ACToR Database
713-68-8
CHEBI ID
CHEBI:39263
CompTox Database
DTXSID9061047
Related Proteins
PDB Bank
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6XQ6
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6XQ8
Molecule Details
MP Biomedicals
05205001
MP Biomedicals Rare Chemical collection
Sigma Aldrich
269980
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem SID
•
PubChem CID
•
MDL Number
•
CAS Number
•
EC Number
•
CHEMBL
•
SureChEMBL Database
•
Protein Data Bank
•
Beilstein Number
•
ACToR Database
•
CHEBI ID
•
CompTox Database
Properties
Safety Information
Storage Warning
Harmful/Irritant
Source
MSDS Link
Download link
Source
Download link
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P301+P310
-
P305+P351+P338
-
P302+P352
-
P405
-P501A
Source
22
-
36/37/38
Source
H302
-
H315
-
H319
-
H335
Source
H301
-
H315
-
H319
-
H335
Source
26
-
36
Source
23
-
26
-
36/37
Source
3
Source
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
SM7700000
Source
Harmful (Xn)
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
是
Source
Product Information
Download link
Source
C6H5OC6H4OH
Source
98%
Source
95%
Source
Physical Property
113 °C
Source
235.4 °F
Source
>110°C(230°F)
Source
185 °C/12 mmHg(lit.)
Source
174-176°C/7mm
Source
1.159 g/mL at 25 °C(lit.)
Source
1.159
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
Source
Harmful (X)
Source
Source
Melting Point
41-42 °C(lit.)
Source
41 - 42°C
Source
41-42°C
Source
Refractive Index
n20/D 1.601(lit.)
Source
1.601
Source
Hydrophobicity(logP)
3.573
Source
Risk Statements
GHS Hazard statements
Safety Statements
German water hazard class
GHS Pictograms
RTECS
European Hazard Symbols
Personal Protective Equipment
TSCA Listed
Certificate of Analysis
Linear Formula
Purity
Flash Point
Boiling Point
Density