1-(4-ethoxyphenyl)-2-phenyl-ethanone结构式
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常用名 | 1-(4-ethoxyphenyl)-2-phenyl-ethanone | 英文名 | 1-(4-ethoxyphenyl)-2-phenyl-ethanone |
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| CAS号 | 38495-73-7 | 分子量 | 240.29700 | |
| 密度 | 1.081g/cm3 | 沸点 | 392.4ºC at 760 mmHg | |
| 分子式 | C16H16O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 175.3ºC |
| 英文名 | 1-(4-ethoxyphenyl)-2-phenylethanone |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.081g/cm3 |
|---|---|
| 沸点 | 392.4ºC at 760 mmHg |
| 分子式 | C16H16O2 |
| 分子量 | 240.29700 |
| 闪点 | 175.3ºC |
| 精确质量 | 240.11500 |
| PSA | 26.30000 |
| LogP | 3.51070 |
| InChIKey | VTSGNASCRQVFMA-UHFFFAOYSA-N |
| SMILES | CCOc1ccc(C(=O)Cc2ccccc2)cc1 |
| 折射率 | 1.562 |
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~55%
1-(4-ethoxyphen... 38495-73-7 |
| 文献:Su, Yijin; Sun, Xiang; Wu, Guolin; Jiao, Ning Angewandte Chemie - International Edition, 2013 , vol. 52, # 37 p. 9808 - 9812 Angew. Chem., 2013 , p. 9990 - 9994 |
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~%
1-(4-ethoxyphen... 38495-73-7 |
| 文献:Bockstahler; Wright Journal of the American Chemical Society, 1949 , vol. 71, p. 3760,3761 |
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1-(4-ethoxyphen... 38495-73-7 |
| 文献:Behaghel; Ratz Chemische Berichte, 1939 , vol. 72, p. 1257,1269 |
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~%
1-(4-ethoxyphen... 38495-73-7 |
| 文献:Tiffeneau; Orekhoff; Roger Bulletin de la Societe Chimique de France, 1931 , vol. <4> 49, p. 1757,1761 |
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~%
1-(4-ethoxyphen... 38495-73-7 |
| 文献:Tiffeneau; Orekhoff; Roger Bulletin de la Societe Chimique de France, 1931 , vol. <4> 49, p. 1757,1761 |
| 1-(4-ethoxyphenyl)-2-phenyl-ethanone上游产品 8 | |
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| 1-(4-ethoxyphenyl)-2-phenyl-ethanone下游产品 1 | |
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
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实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标: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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实验名称:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
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