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Molecule
ID:10622
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₇IO₂
Molecular Mass
262.04445
Exact Mass
261.94907746
Charge
0
InChI
InChI=1S/C8H7IO2/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4H,5H2,(H,10,11)
InChIKey
MRSWWBAFGGGWRH-UHFFFAOYSA-N
Canonic Smiles
OC(=O)Cc1cccc(c1)I
Isomeric Smiles
c1cc(cc(c1)CC(=O)O)I
Calculated Properties
JChem
Acid pKa
3.2003949
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.2630165
LogD (pH = 7.4)
-0.9054349
Log P
2.5399387
Molar Refractivity
50.7281
Polarizability
19.78427
Polar Surface Area
37.3
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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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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Safety Information
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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
Apollo Scientific
OR18733
Matrix Scientific
007466
MP Biomedicals
05212530
Sigma Aldrich
587001
Alfa Aesar
L15117
Chemik
CHB15700
Enamine
EN300-103230
Bide Pharmatech
BD6172
Academic Data
PubChem
3870220
Names and Identifiers
IUPAC name
2-(3-iodophenyl)acetic acid
Synonyms
3-Iodophenylacetic acid
m-IODOPHENYLACETIC ACID
3-碘苯乙酸
3-Iodophenylacetic acid
2-(3-iodophenyl)acetic acid
IUPAC Traditional name
M-iodophenylacetic acid
Registration numbers
PubChem CID
3870220
PubChem SID
160973929
24881151
MDL Number
MFCD00046548
CAS Number
1878-69-9
EC Number
000-000-0
Beilstein Number
2501867
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Storage Warning
IRRITANT, LIGHT SENSITIVE
Source
Irritant/Light Sensitive
Source
Light Sensitive
Source
TSCA Listed
false
Source
否
Source
GHS Signal Word
Warning
Source
Safety Statements
26
-
36
Source
26
-
37
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
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
Risk Statements
36/37/38
Source
German water hazard class
3
Source
Product Information
Purity
98%
Source
95%
Source
Certificate of Analysis
Download link
Source
Linear Formula
IC6H4CH2CO2H
Source
Physical Property
Melting Point
129-131°C
Source
128-132°C
Source
128°C
Source
127-131 °C(lit.)
Source
124 - 126°C
Source
128-132°C
Source
Hydrophobicity(logP)
2.537
Source
Molecule Details
Sigma Aldrich
587001
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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PubChem CID
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PubChem SID
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MDL Number
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CAS Number
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EC Number
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Beilstein Number