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Molecule
ID:61311
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₇H₁₄O₄
Molecular Mass
282.29066
Exact Mass
282.08920893
Charge
0
InChI
InChI=1S/C17H14O4/c1-10-16(11-3-6-13(20-2)7-4-11)17(19)14-8-5-12(18)9-15(14)21-10/h3-9,18H,1-2H3
InChIKey
LEVXOZABOPNCSR-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cc1)c1c(C)oc2c(c1=O)ccc(c2)O
Isomeric Smiles
c1(c(=O)c2c(oc1C)cc(cc2)O)c1ccc(cc1)OC
Calculated Properties
JChem
Acid pKa
6.469747
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
3.0344968
LogD (pH = 7.4)
2.1249416
Log P
3.0784044
Molar Refractivity
80.0034
Polarizability
30.227749
Polar Surface Area
55.76
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
066513
InterBioScreen
STOCK1N-30427
Enamine
EN300-03241
Academic Data
PubChem
5400231
Names and Identifiers
Synonyms
7-Hydroxy-3-(4-methoxyphenyl)-2-methyl-4H-chromen-4-one
IUPAC name
7-hydroxy-3-(4-methoxyphenyl)-2-methyl-4H-chromen-4-one
IUPAC Traditional name
7-hydroxy-3-(4-methoxyphenyl)-2-methylchromen-4-one
Registration numbers
MDL Number
MFCD01995502
CAS Number
13004-42-7
PubChem CID
5400231
PubChem SID
162027052
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
TSCA Listed
false
Source
Product Information
Classification
Derivatives & analogs of Natural Compounds
Source
Purity
95%
Source
Physical Property
Hydrophobicity(logP)
2.843
Source
Melting Point
282 - 284°C
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay