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Molecule
ID:8663
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/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4H,1H3,(H,10,11)
InChIKey
INGWGCDYAJKXKP-UHFFFAOYSA-N
Canonic Smiles
Cc1ccc(c(c1)C(=O)O)I
Isomeric Smiles
c1(ccc(c(c1)C(=O)O)I)C
Calculated Properties
JChem
Acid pKa
3.3027687
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.8929673
LogD (pH = 7.4)
-0.35231838
Log P
3.0731945
Molar Refractivity
51.7179
Polarizability
19.697454
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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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
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RDKit
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IUPAC name
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MDL Number
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR2196
Matrix Scientific
004488
Enamine
EN300-62484
Bide Pharmatech
BD75989
A&J Pharmtech
AJA-O2485
Academic Data
PubChem
142941
Names and Identifiers
Synonyms
2-Iodo-5-methylbenzoic acid
3-Carboxy-4-iodotoluene
IUPAC Traditional name
2-iodo-5-methylbenzoic acid
IUPAC name
2-iodo-5-methylbenzoic acid
Registration numbers
CAS Number
52548-14-8
PubChem SID
160971970
PubChem CID
142941
MDL Number
MFCD00079765
Properties
Safety Information
MSDS Link
Download link
Source
TSCA Listed
false
Source
Storage Warning
LIGHT SENSITIVE
Source
Irritant
Source
Product Information
Purity
98%
Source
95%
Source
97%
Source
Physical Property
Melting Point
122-124°C
Source
119 - 121°C
Source
Hydrophobicity(logP)
2.895
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay