1-苯基咪唑-2-酮

• 常用名: 1-苯基咪唑-2-酮
• 英文名: 1-Phenyl-2-imidazolidinone
• CAS号: 1848-69-7
• 分子量: 162.189
• 密度: 1.2±0.1 g/cm3
• 沸点: N/A
• 分子式: C₉H₁₀N₂O
• 熔点: N/A
• 闪点: N/A

1-苯基咪唑-2-酮名称

• 中文名: 1-苯基咪唑啉-2-酮
• 英文名: 1-phenylimidazolidin-2-one
• 中文别名: 1-苯基咪唑-2-酮

1-苯基咪唑-2-酮物理化学性质

• 密度: 1.2±0.1 g/cm3
• 分子式: C₉H₁₀N₂O
• 分子量: 162.189
• 精确质量: 162.079315
• PSA: 32.34000
• LogP: 0.49
• InChIKey: QKKGTRSHKSWYAK-UHFFFAOYSA-N
• SMILES: O=C1NCCN1c1ccccc1
• 折射率: 1.578

1-苯基咪唑-2-酮安全信息

• 危害码 (欧洲): Xi: Irritant;
• 海关编码: 2933990090

1-苯基咪唑-2-酮海关

• 海关编码: 2933990090
• 中文概述: 2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
• 申报要素: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期
• Summary: 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

1-苯基咪唑-2-酮靶点实验

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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

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：High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce... 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School 靶标：N/A External Id：HMS1149-MLP

实验名称：qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima... 来源：NCGC 靶标：apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7] External Id：AMA1100

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1-苯基咪唑-2-酮英文别名

• 2-oxo-1-phenyl-imidazolidine
• 1-Phenyl-2-imidazolidinone
• 1-Phenyl-imidazolidin-2-on
• 1-phenyl-2-imidazolidinon
• 3-Phenyl-2-imidazolidinone
• 1-Phenylimidazolidin-2-one
• 1-phenyl-imidazolidin-2-one
• 2-Imidazolidinone,1-phenyl
• 4,5-dihydro-1-phenylimidazol-2(1H)-one
• N-phenyl-imidazolidinone