2(5H)-Furanone,4-phenyl
Modify Date: 2025-08-23 18:36:21
2(5H)-Furanone,4-phenyl structure
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Common Name | 2(5H)-Furanone,4-phenyl | ||
|---|---|---|---|---|
| CAS Number | 1575-47-9 | Molecular Weight | 160.16900 | |
| Density | 1.215g/cm3 | Boiling Point | 338.8ºC at 760mmHg | |
| Molecular Formula | C10H8O2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 140.6ºC | |
| Name | 3-phenyl-2H-furan-5-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.215g/cm3 |
|---|---|
| Boiling Point | 338.8ºC at 760mmHg |
| Molecular Formula | C10H8O2 |
| Molecular Weight | 160.16900 |
| Flash Point | 140.6ºC |
| Exact Mass | 160.05200 |
| PSA | 26.30000 |
| LogP | 1.62680 |
| Vapour Pressure | 9.6E-05mmHg at 25°C |
| Index of Refraction | 1.586 |
| InChIKey | HJJHMYDTEVUBHZ-UHFFFAOYSA-N |
| SMILES | O=C1C=C(c2ccccc2)CO1 |
| Precursor 7 | |
|---|---|
| DownStream 2 | |
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
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Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
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| 4-Phenyl-5H-furan-2-on |
| 4-phenyl-5H-furan-2-one |
| 2(5H)-Furanone,4-phenyl |
| 4-phenyl-2(5H)-furanone |
| 4-phenyl-5H-furanone |
| 4-phenylfuran-2(5H)-one |