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Molecule
ID:119821
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₁₀O₃
Molecular Mass
238.2381
Exact Mass
238.06299418
Charge
0
InChI
InChI=1S/C15H10O3/c16-12-7-6-11-8-13(10-4-2-1-3-5-10)15(17)18-14(11)9-12/h1-9,16H
InChIKey
RIPZCQZTVDNJHQ-UHFFFAOYSA-N
Canonic Smiles
Oc1ccc2c(c1)oc(=O)c(c2)c1ccccc1
Isomeric Smiles
c1(=O)c(cc2c(o1)cc(cc2)O)c1ccccc1
Calculated Properties
JChem
Acid pKa
7.7758193
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
3.1456015
LogD (pH = 7.4)
2.9964705
Log P
3.147882
Molar Refractivity
67.9816
Polarizability
25.958218
Polar Surface Area
46.53
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
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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
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IUPAC name
Registration numbers
Properties
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Safety Information
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Physical Property
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Product Information
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Pharmacology Properties
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
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PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_NC-1950
STOCK1N-70900
Sigma Aldrich
79279
Enamine
EN300-36438
Academic Data
PubChem
5393176
Names and Identifiers
Synonyms
7-hydroxy-3-phenyl-2H-chromen-2-one
3-Phenylumbelliferone
7-Hydroxy-3-phenylcoumarin
IUPAC Traditional name
7-hydroxy-3-phenylchromen-2-one
IUPAC name
7-hydroxy-3-phenyl-2H-chromen-2-one
Registration numbers
PubChem SID
24887436
162107930
Beilstein Number
384125
CAS Number
6468-96-8
MDL Number
MFCD00037574
PubChem CID
5393176
Molecule Details
Sigma Aldrich
79279
Application
suitable as pH-indicator
Other Notes
Fluorescent pH probe for the physiological pH range1
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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PubChem SID
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Beilstein Number
•
CAS Number
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MDL Number
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PubChem CID
Properties
Safety Information
MSDS Link
Download link
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Physical Property
Solubility
alcohols: soluble
Source
DMSO: soluble
Source
DMF: soluble
Source
7.8
Source
λex 338 nm; λem 463 nm (pH 3.0)
Source
λex 383 nm; λem 472 nm in 0.1 M Tris pH 9.0
Source
206-210 °C(lit.)
Source
3.721
Source
Product Information
≥98.0% (TLC)
Source
95%
Source
C15H10O3
Source
suitable for fluorescence
Source
Derivatives & analogs of Natural Compounds
Source
Pharmacology Properties
human ... MIF(4282)
Source
p𝘒ₐ
Fluorescence
Melting Point
Hydrophobicity(logP)
Purity
Empirical Formula (Hill Notation)
Suitability
Classification
Gene Information