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Molecule
ID:114105
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₈N₂O₄
Molecular Mass
220.18152
Exact Mass
220.04840675
Charge
0
InChI
InChI=1S/C10H8N2O4/c13-9-4-3-7(8-2-1-5-16-8)11-12(9)6-10(14)15/h1-5H,6H2,(H,14,15)
InChIKey
BOVLYDIHHNLNCR-UHFFFAOYSA-N
Canonic Smiles
OC(=O)Cn1nc(ccc1=O)c1ccco1
Isomeric Smiles
n1(nc(c2occc2)ccc1=O)CC(=O)O
Calculated Properties
JChem
Acid pKa
3.5862715
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
-1.78681
LogD (pH = 7.4)
-3.2259924
Log P
0.12178859
Molar Refractivity
54.0756
Polarizability
19.86541
Polar Surface Area
83.11
Rotatable Bonds
3
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
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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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IUPAC name
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IUPAC Traditional name
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PubChem SID
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MDL Number
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PubChem CID
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Physical Property
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Life Chemicals
F1967-0190
InterBioScreen
BB_SC-9128
Academic Data
PubChem
33675951
Names and Identifiers
Synonyms
[3-(2-furyl)-6-oxopyridazin-1(6{H})-yl]acetic acid
2-(3-(furan-2-yl)-6-oxopyridazin-1(6H)-yl)acetic acid
IUPAC name
2-[3-(furan-2-yl)-6-oxo-1,6-dihydropyridazin-1-yl]acetic acid
IUPAC Traditional name
[3-(furan-2-yl)-6-oxopyridazin-1-yl]acetic acid
Registration numbers
PubChem SID
162100540
MDL Number
MFCD16652644
PubChem CID
33675951
Properties
Product Information
Purity
95+%
Source
Physical Property
Partition Coefficient
-0.056
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay