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Molecule
ID:110859
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₉N
Molecular Mass
143.18516
Exact Mass
143.07349929
Charge
0
InChI
InChI=1S/C10H9N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h1-9H
InChIKey
GEZGAZKEOUKLBR-UHFFFAOYSA-N
Canonic Smiles
c1ccc(cc1)n1cccc1
Isomeric Smiles
c1ccc(cc1)n1cccc1
Calculated Properties
JChem
H Acceptors
0
H Donor
0
LogD (pH = 5.5)
2.9347644
LogD (pH = 7.4)
2.9347644
Log P
2.9347644
Molar Refractivity
55.8104
Polarizability
18.412361
Polar Surface Area
4.93
Rotatable Bonds
1
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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Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
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Physical Property
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Molecular Spectra
Molecule Details
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MP Biomedicals
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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
Alfa Aesar
L07973
MP Biomedicals
05216648
Sigma Aldrich
131474
Academic Data
PubChem
12480
Names and Identifiers
IUPAC name
1-phenyl-1H-pyrrole
Synonyms
1-Phenylpyrrole
1-苯基吡咯
(1-Pyrrolyl)benzene
N-PHENYLPYRROLE
IUPAC Traditional name
pyrrole, 1-phenyl-
Registration numbers
EC Number
211-242-3
MDL Number
MFCD00005343
Beilstein Number
109798
CAS Number
635-90-5
PubChem CID
12480
PubChem SID
162096039
24848017
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
GHS Signal Word
Warning
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Safety Statements
26
-
37/39
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
36/37/38
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
German water hazard class
3
Source
TSCA Listed
否
Source
Product Information
Certificate of Analysis
Download link
Source
Purity
99%
Source
Empirical Formula (Hill Notation)
C10H9N
Source
Physical Property
Melting Point
58-60 °C(lit.)
Source
57-60°C
Source
Boiling Point
234 °C(lit.)
Source
131°C/30mm
Source
Molecule Details
MP Biomedicals
05216648
MP Biomedicals Rare Chemical collection
Sigma Aldrich
131474
Packaging
10, 25 g in glass bottle
References
PubChem Literature
From Data Sources
•
Lithiation occurs preferentially at the 2-position of the pyrrole ring, but can also take place at the ortho-position of the benzene ring. For a detailed study, see:
Tetrahedron
,
49
, 10271 (1993).
Bioactivity
PubChem BioAssay
Registration numbers
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EC Number
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MDL Number
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Beilstein Number
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CAS Number
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PubChem CID
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PubChem SID