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2-phenyl-5,6-dihydro-4H-1,3-oxazine

更新时间:2025-08-30 10:20:08

2-phenyl-5,6-dihydro-4H-1,3-oxazine结构式
2-phenyl-5,6-dihydro-4H-1,3-oxazine结构式
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常用名 2-phenyl-5,6-dihydro-4H-1,3-oxazine 英文名 2-phenyl-5,6-dihydro-4H-1,3-oxazine
CAS号 3420-41-5 分子量 161.20000
密度 1.09g/cm3 沸点 271.9ºC at 760 mmHg
分子式 C10H11NO 熔点 N/A
MSDS N/A 闪点 98.1ºC

 2-phenyl-5,6-dihydro-4H-1,3-oxazine名称

英文名 2-phenyl-5,6-dihydro-4H-1,3-oxazine
英文别名 更多

 2-phenyl-5,6-dihydro-4H-1,3-oxazine物理化学性质

密度 1.09g/cm3
沸点 271.9ºC at 760 mmHg
分子式 C10H11NO
分子量 161.20000
闪点 98.1ºC
精确质量 161.08400
PSA 21.59000
LogP 1.28910
InChIKey GUXASSGFGULBAX-UHFFFAOYSA-N
SMILES c1ccc(C2=NCCCO2)cc1
折射率 1.563

 2-phenyl-5,6-dihydro-4H-1,3-oxazine合成线路

 2-phenyl-5,6-dihydro-4H-1,3-oxazine靶点实验

查看更多实验

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
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
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
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
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
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
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
实验名称:Inhibition of rabbit muscle glycogen phosphorylase a assessed as inhibition of releas...
来源:ChEMBL
靶标:Glycogen phosphorylase, muscle form
External Id:CHEMBL3369653
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
实验名称:GPR151 activator identification: cell-based high-throughput counter-screen assay
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Glucose-dependent insulinotropic receptor; AltName: Full=G-protein coupled receptor 119
External Id:GPR119_PHUNTER_AG_LUMI_1536_3X%ACT CSRUN1
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 2-phenyl-5,6-dihydro-4H-1,3-oxazine英文别名

2-phenyloxazine
5,6-dihydro-2-phenyl-4H-1,3-oxazine
2-phenyl-4,5-dihydro-1,3-oxazine
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