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Molecule
ID:8662
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General Information
Structure
Molecular Formula
C₈H₇IO₂
Molecular Mass
262.04445
Exact Mass
261.94907746
Charge
0
InChI
InChI=1S/C8H7IO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4H,1H3,(H,10,11)
InChIKey
PZUXUOZSSYKAMX-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1cccc(c1I)C
Isomeric Smiles
c1cc(c(c(c1)C(=O)O)I)C
Calculated Properties
JChem
Acid pKa
3.3052795
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.8953508
LogD (pH = 7.4)
-0.3517827
Log P
3.0731945
Molar Refractivity
51.7179
Polarizability
19.699102
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
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
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
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Physical Property
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Safety Information
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Product Information
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
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
004487
Sigma Aldrich
560499
Alfa Aesar
L19876
Enamine
EN300-39534
Bide Pharmatech
BD75969
A&J Pharmtech
AJA-O781
Academic Data
PubChem
2759365
Names and Identifiers
Synonyms
2-Iodo-3-methylbenzoic acid
2-Iodo-m-toluic acid
2-碘-3-甲基苯甲酸
2-Iodo-3-methylbenzoic acid
IUPAC Traditional name
2-iodo-3-methylbenzoic acid
IUPAC name
2-iodo-3-methylbenzoic acid
Registration numbers
CAS Number
108078-14-4
PubChem SID
24879870
160971969
MDL Number
MFCD00079764
EC Number
000-000-0
Beilstein Number
2439521
PubChem CID
2759365
Properties
Physical Property
Melting Point
150-153°C
Source
150-153 °C(lit.)
Source
150-153°C
Source
Hydrophobicity(logP)
2.595
Source
Safety Information
Storage Warning
LIGHT SENSITIVE
Source
Light Sensitive
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
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 Hazard statements
H315
-
H319
-
H335
Source
Safety Statements
26
-
37
Source
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Risk Statements
36/37/38
Source
European Hazard Symbols
Irritant (Xi)
Source
Product Information
Purity
98%
Source
97%
Source
95%
Source
Linear Formula
IC6H3(CH3)CO2H
Source
Molecule Details
Sigma Aldrich
560499
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
PubChem SID
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MDL Number
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EC Number
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Beilstein Number
•
PubChem CID