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Molecule
ID:21712
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/c1-5-2-3-6(8(10)11)4-7(5)9/h2-4H,1H3,(H,10,11)
InChIKey
LDDHMKANNXWUAK-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1ccc(c(c1)I)C
Isomeric Smiles
C(=O)(c1cc(c(cc1)C)I)O
Calculated Properties
JChem
Acid pKa
4.1491427
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
1.7062644
LogD (pH = 7.4)
0.0057873703
Log P
3.0731945
Molar Refractivity
51.7179
Polarizability
19.695335
Polar Surface Area
37.3
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
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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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IUPAC name
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IUPAC Traditional name
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Physical Property
Related Proteins
Molecular Spectra
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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
OR17850
Matrix Scientific
024059
Sigma Aldrich
278858
Enamine
EN300-68156
Bide Pharmatech
BD8183
Alfa Aesar
A14197
Academic Data
PubChem
621640
Names and Identifiers
Synonyms
3-Iodo-4-methylbenzoic acid
3-Iodo-4-methylbenzoic acid
3-Iodo-p-toluic acid
3-碘-4-甲基苯甲酸
4-Carboxy-2-iodotoluene
IUPAC name
3-iodo-4-methylbenzoic acid
IUPAC Traditional name
3-iodo-4-methylbenzoic acid
Registration numbers
Beilstein Number
2436216
MDL Number
MFCD00010392
CAS Number
82998-57-0
PubChem SID
24856837
160985019
PubChem CID
621640
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant/Light Sensitive/Keep Cold
Source
Light Sensitive
Source
TSCA Listed
false
Source
否
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
Safety Statements
26
-
37/39
Source
26
-
37
Source
Risk Statements
36/37/38
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
European Hazard Symbols
Irritant (Xi)
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
German water hazard class
3
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Signal Word
Warning
Source
Product Information
Purity
97%
Source
95%
Source
98%
Source
Linear Formula
IC6H3(CH3)CO2H
Source
Physical Property
Melting Point
210-212°C
Source
210-212 °C(lit.)
Source
200 - 202°C
Source
206-210°C
Source
Hydrophobicity(logP)
3.305
Source
Molecule Details
Sigma Aldrich
278858
Packaging
5, 25 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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Beilstein Number
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MDL Number
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CAS Number
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PubChem SID
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PubChem CID