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Molecule
ID:8031
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₇IO
Molecular Mass
246.04505
Exact Mass
245.95416284
Charge
0
InChI
InChI=1S/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3
InChIKey
JZJWCDQGIPQBAO-UHFFFAOYSA-N
Canonic Smiles
CC(=O)c1ccc(cc1)I
Isomeric Smiles
O=C(C)c1ccc(cc1)I
Calculated Properties
JChem
Acid pKa
16.06177
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.459838
LogD (pH = 7.4)
2.459838
Log P
2.459838
Molar Refractivity
49.8233
Polarizability
19.213692
Polar Surface Area
17.07
Rotatable Bonds
1
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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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
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Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
•
Product Information
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Physical Property
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR7749
InterBioScreen
BB_SC-8802
Matrix Scientific
003426
Sigma Aldrich
357804
Bide Pharmatech
BD11067
Alfa Aesar
A16794
Academic Data
PubChem
72869
Names and Identifiers
Synonyms
4'-Iodoacetophenone
1-(4-iodophenyl)ethanone
1-(4-Iodophenyl)-1-oxoethane
1-(4-Iodophenyl)ethan-1-one
4′-碘苯乙酮
4′-Iodoacetophenone
4'-碘苯乙酮
4'-Iodoacetophenone
IUPAC Traditional name
1-(4-iodo-phenyl)-ethanone
IUPAC name
1-(4-iodophenyl)ethan-1-one
Registration numbers
PubChem SID
160971338
24861945
PubChem CID
72869
EC Number
236-372-8
MDL Number
MFCD00045320
CAS Number
13329-40-3
Beilstein Number
1857412
Molecule Details
Sigma Aldrich
357804
Packaging
25 g in poly bottle
5 g in glass bottle
Application
Convenient substrate for palladium-catalyzed coupling reactions.1 Used in the synthesis of quinoline-based potential anticancer agents.2
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem SID
•
PubChem CID
•
EC Number
•
MDL Number
•
CAS Number
•
Beilstein Number
Properties
Product Information
Purity
98%
Source
Linear Formula
IC6H4COCH3
Source
Physical Property
Melting Point
85-87°C
Source
82-84°C
Source
82-84 °C(lit.)
Source
82-84°C
Source
Safety Information
false
Source
否
Source
Download link
Source
Download link
Source
IRRITANT
Source
Irritant/Light Sensitive
Source
Light Sensitive
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
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
GHS Signal Word
Warning
Source
Safety Statements
26
-
37/39
Source
26
-
37
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
TSCA Listed
MSDS Link
Storage Warning