(4-甲基-香豆素-7-基氧代)乙酸乙酯结构式
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常用名 | (4-甲基-香豆素-7-基氧代)乙酸乙酯 | 英文名 | ethyl 2-(4-methyl-2-oxo-chromen-7-yl)oxyacetate |
|---|---|---|---|---|
| CAS号 | 5614-82-4 | 分子量 | 262.25800 | |
| 密度 | 1.236g/cm3 | 沸点 | 413.5ºC at 760 mmHg | |
| 分子式 | C14H14O5 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 184.8ºC |
| 中文名 | (4-甲基-香豆素-7-基氧代)乙酸乙酯 |
|---|---|
| 英文名 | ethyl 2-(4-methyl-2-oxochromen-7-yl)oxyacetate |
| 密度 | 1.236g/cm3 |
|---|---|
| 沸点 | 413.5ºC at 760 mmHg |
| 分子式 | C14H14O5 |
| 分子量 | 262.25800 |
| 闪点 | 184.8ºC |
| 精确质量 | 262.08400 |
| PSA | 65.74000 |
| LogP | 2.04330 |
| InChIKey | FPDRQKTUWRSVPL-UHFFFAOYSA-N |
| SMILES | CCOC(=O)COc1ccc2c(C)cc(=O)oc2c1 |
| 折射率 | 1.542 |
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~95%
(4-甲基-香豆素-7-基氧代)乙酸乙酯 5614-82-4 |
| 文献:Chimichi, Stefano; Boccalini, Marco; Cosimelli, Barbara Tetrahedron, 2002 , vol. 58, # 24 p. 4851 - 4858 |
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~98%
(4-甲基-香豆素-7-基氧代)乙酸乙酯 5614-82-4 |
| 文献:Zav'yalov; Dorofeeva; Rumyantseva; Kulikova; Ezhova; Kravchenko; Zavozin Pharmaceutical Chemistry Journal, 1998 , vol. 32, # 3 p. 154 - 156 |
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~91%
(4-甲基-香豆素-7-基氧代)乙酸乙酯 5614-82-4 |
| 文献:Sheng, Shou-Ri; Huang, Pei-Gang; Wang, Qiong; Huang, Ren; Liu, Xiao-Ling Synthetic Communications, 2006 , vol. 36, # 21 p. 3175 - 3181 |
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~86%
(4-甲基-香豆素-7-基氧代)乙酸乙酯 5614-82-4 |
| 文献:Valizadeh, Hassan; Shockravi, Abbas Tetrahedron Letters, 2005 , vol. 46, # 20 p. 3501 - 3503 |
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~%
(4-甲基-香豆素-7-基氧代)乙酸乙酯 5614-82-4 |
| 文献:Satyanarayana; Rakshit, Madhumita; Sivakumar Asian Journal of Chemistry, 2011 , vol. 23, # 3 p. 1295 - 1301 |
| (4-甲基-香豆素-7-基氧代)乙酸乙酯上游产品 7 | |
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| (4-甲基-香豆素-7-基氧代)乙酸乙酯下游产品 3 | |
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实验名称:Cytotoxicity against human T24 cells assessed as reduction of cell viability at 5 to ...
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL3744125
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实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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实验名称:Inhibitors of CDC25B-CDK2/CyclinA interaction
来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
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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:Antiasthamic activity in Wistar rat tracheal ring assessed as reversal of carbachol-i...
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL3269356
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
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实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
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