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Molecule
ID:70976
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₉NO
Molecular Mass
183.20596
Exact Mass
183.06841391
Charge
0
InChI
InChI=1S/C12H9NO/c14-12(10-5-2-1-3-6-10)11-7-4-8-13-9-11/h1-9H
InChIKey
RYMBAPVTUHZCNF-UHFFFAOYSA-N
Canonic Smiles
O=C(c1cccnc1)c1ccccc1
Isomeric Smiles
C(=O)(c1cnccc1)c1ccccc1
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
2.2083511
LogD (pH = 7.4)
2.2148428
Log P
2.2149265
Molar Refractivity
54.4766
Polarizability
21.095764
Polar Surface Area
29.96
Rotatable Bonds
2
Lipinski's Rule of Five
true
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
No Data Available
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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
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC Traditional name
•
IUPAC name
•
Synonyms
Registration numbers
Properties
•
Product Information
•
Safety Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
MP Biomedicals
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR30455
MP Biomedicals
05209633
InterBioScreen
BB_SC-2581
Matrix Scientific
076551
Sigma Aldrich
B14205
Enamine
EN300-26771
Bide Pharmatech
BD41785
Alfa Aesar
A16695
A&J Pharmtech
AJA-O1800
Academic Data
PubChem
21540
Names and Identifiers
IUPAC Traditional name
phenyl-B-pyridyl ketone
IUPAC name
3-benzoylpyridine
Synonyms
3-Benzoylpyridine 97%
3-BENZOYLPYRIDINE
Phenyl(pyridin-3-yl)methanone
3-苯甲酰基吡啶
3-Benzoylpyridine
Phenyl 3-pyridyl ketone
3-苯甲酰吡啶
Registration numbers
CAS Number
5424-19-1
MDL Number
MFCD00006394
PubChem CID
21540
PubChem SID
162036684
24891593
Beilstein Number
120234
EC Number
226-561-3
Molecule Details
MP Biomedicals
05209633
MP Biomedicals Rare Chemical collection
Sigma Aldrich
B14205
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem CID
•
PubChem SID
•
Beilstein Number
•
EC Number
Properties
Product Information
Purity
95+%
Source
97%
Source
95%
Source
98%
Source
98+%
Source
Certificate of Analysis
Download link
Source
Empirical Formula (Hill Notation)
C12H9NO
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
否
Source
OB6401000
Source
Irritant (Xi)
R:
36/37/38
Source
36/37/38
Source
S:
20
-
25
-
26
-
37/39
Source
26
-
37/39
Source
26
-
37
dust mask type N95 (US), Eyeshields, Gloves
Source
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
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
Warning
Source
H315
-
H319
-
H335
Source
3
Source
Physical Property
Flash Point
150 °C
Source
302 °F
Source
150°C(302°F)
Source
Melting Point
36-40 °C(lit.)
Source
36 - 40°C
Source
36-40°C
Source
Boiling Point
307 °C(lit.)
Source
307°C
Source
2.079
Source
Source
Source
Source
RTECS
European Hazard Symbols
Risk Statements
Safety Statements
Personal Protective Equipment
GHS Precautionary statements
GHS Pictograms
GHS Signal Word
GHS Hazard statements
German water hazard class
Hydrophobicity(logP)