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Molecule
ID:24618
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₃IO₂
Molecular Mass
221.98059
Exact Mass
221.91777734
Charge
0
InChI
InChI=1S/C5H3IO2/c6-5-2-1-4(3-7)8-5/h1-3H
InChIKey
QPGPCPKDVSPJAY-UHFFFAOYSA-N
Canonic Smiles
Ic1ccc(o1)C=O
Isomeric Smiles
c1(oc(cc1)C=O)I
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
1.737338
LogD (pH = 7.4)
1.737338
Log P
1.737338
Molar Refractivity
36.6943
Polarizability
14.677661
Polar Surface Area
30.21
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
•
RDKit
•
JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
•
IUPAC name
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Synonyms
Registration numbers
Properties
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Safety Information
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Physical Property
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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
027125
Apollo Scientific
OR8105
Sigma Aldrich
579289
Enamine
EN300-41081
Alfa Aesar
L19670
Academic Data
PubChem
693264
Names and Identifiers
IUPAC Traditional name
5-iodofuran-2-carbaldehyde
IUPAC name
5-iodofuran-2-carbaldehyde
Synonyms
5-Iodo-2-furaldehyde
5-Iodofuran-2-carboxaldehyde 95%
5-碘-2-呋喃甲醛
5-Iodo-2-furaldehyde
5-Iodofurfural
5-Iodofuran-2-carboxaldehyde
5-碘糠醛
Registration numbers
PubChem CID
693264
PubChem SID
160987925
24880982
CAS Number
2689-65-8
MDL Number
MFCD00159503
Beilstein Number
108406
EC Number
000-000-0
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
Air & Light Sensitive
Source
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Safety Statements
26
-
36/37
Source
26
-
37
Source
GHS Signal Word
Warning
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 Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
European Hazard Symbols
Irritant (Xi)
Source
Physical Property
Melting Point
93°C
Source
125-128 °C(lit.)
Source
93 - 95°C
Source
126-127°C
Source
Hydrophobicity(logP)
1.917
Source
Product Information
Empirical Formula (Hill Notation)
C5H3IO2
Source
Purity
97%
Source
95%
Source
Molecule Details
Sigma Aldrich
579289
Packaging
1 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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CAS Number
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MDL Number
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Beilstein Number
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EC Number