2H-1-Benzopyran-7-ol,3-[4-(acetyloxy)phenyl]-2-methyl-, 7-acetate structure
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Common Name | 2H-1-Benzopyran-7-ol,3-[4-(acetyloxy)phenyl]-2-methyl-, 7-acetate | ||
|---|---|---|---|---|
| CAS Number | 10499-08-8 | Molecular Weight | 338.35400 | |
| Density | 1.216g/cm3 | Boiling Point | 472.1ºC at 760mmHg | |
| Molecular Formula | C20H18O5 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 207.4ºC | |
| Name | [4-(7-acetyloxy-2-methyl-2H-chromen-3-yl)phenyl] acetate |
|---|---|
| Synonym | More Synonyms |
| Density | 1.216g/cm3 |
|---|---|
| Boiling Point | 472.1ºC at 760mmHg |
| Molecular Formula | C20H18O5 |
| Molecular Weight | 338.35400 |
| Flash Point | 207.4ºC |
| Exact Mass | 338.11500 |
| PSA | 61.83000 |
| LogP | 3.85870 |
| Vapour Pressure | 4.4E-09mmHg at 25°C |
| Index of Refraction | 1.571 |
| InChIKey | DNZGBFXOVKCJMO-UHFFFAOYSA-N |
| SMILES | CC(=O)Oc1ccc(C2=Cc3ccc(OC(C)=O)cc3OC2C)cc1 |
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~72%
2H-1-Benzopyran... CAS#:10499-08-8 |
| Literature: NOVOGEN RESEARCH PTY LTD Patent: WO2009/3229 A1, 2009 ; Location in patent: Page/Page column 35-36 ; WO 2009/003229 A1 |
| Precursor 2 | |
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| DownStream 0 | |
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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: High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS1149-MLP
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Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
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| HMS3079M13 |
| 4',7-diacetoxy-2-methyl-isoflav-3-ene |