4-苯基-1H-2,3-苯并嗪-1-酮结构式
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常用名 | 4-苯基-1H-2,3-苯并嗪-1-酮 | 英文名 | 7-phenyl-9-oxa-8-azabicyclo[4.4.0]deca-1,3,5,7-tetraen-10-one |
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| CAS号 | 19298-29-4 | 分子量 | 223.22700 | |
| 密度 | 1.23g/cm3 | 沸点 | 379.8ºC at 760 mmHg | |
| 分子式 | C14H9NO2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 185.6ºC |
| 中文名 | 4-苯基-1H-2,3-苯并嗪-1-酮 |
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| 英文名 | 4-phenyl-2,3-benzoxazin-1-one |
| 英文别名 | 更多 |
| 密度 | 1.23g/cm3 |
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| 沸点 | 379.8ºC at 760 mmHg |
| 分子式 | C14H9NO2 |
| 分子量 | 223.22700 |
| 闪点 | 185.6ºC |
| 精确质量 | 223.06300 |
| PSA | 43.10000 |
| LogP | 2.85500 |
| InChIKey | FUSZISDRVACNBS-UHFFFAOYSA-N |
| SMILES | O=c1onc(-c2ccccc2)c2ccccc12 |
| 蒸汽压 | 5.7E-06mmHg at 25°C |
| 折射率 | 1.634 |
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~93%
4-苯基-1H-2,3-苯并嗪-1-酮 19298-29-4 |
| 文献:Bansal, R. K.; Kumar, Girijesh; Jain, S. K.; Puri, B. K. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1988 , vol. 27, # 1-12 p. 1045 |
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~%
4-苯基-1H-2,3-苯并嗪-1-酮 19298-29-4 |
| 文献:Watanabe,H. et al. Journal of Organic Chemistry, 1969 , vol. 34, # 6 p. 1786 - 1791 |
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~%
4-苯基-1H-2,3-苯并嗪-1-酮 19298-29-4 |
| 文献:Watanabe,H. et al. Journal of Organic Chemistry, 1969 , vol. 34, # 6 p. 1786 - 1791 |
| 4-苯基-1H-2,3-苯并嗪-1-酮上游产品 2 | |
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| 4-苯基-1H-2,3-苯并嗪-1-酮下游产品 5 | |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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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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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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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| 4-Phenyl-3.4-dehydro-1-oxo-2.3.1-benzoxazin |
| 4-Phenyl-1H-2,3-benzoxazin-1-one |