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3,4-di(4-morpholinyl)-4-phenyl-2-butanone

更新时间:2025-10-02 06:34:22

3,4-di(4-morpholinyl)-4-phenyl-2-butanone结构式
3,4-di(4-morpholinyl)-4-phenyl-2-butanone结构式
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常用名 3,4-di(4-morpholinyl)-4-phenyl-2-butanone 英文名 3,4-di(4-morpholinyl)-4-phenyl-2-butanone
CAS号 5455-91-4 分子量 318.41100
密度 1.15g/cm3 沸点 429.3ºC at 760 mmHg
分子式 C18H26N2O3 熔点 N/A
MSDS N/A 闪点 213.4ºC

 名称

英文名 3,4-dimorpholin-4-yl-4-phenylbutan-2-one
英文别名 更多

 物理化学性质

密度 1.15g/cm3
沸点 429.3ºC at 760 mmHg
分子式 C18H26N2O3
分子量 318.41100
闪点 213.4ºC
精确质量 318.19400
PSA 42.01000
LogP 1.22550
InChIKey VXZFZOFWTCDDNB-UHFFFAOYSA-N
SMILES CC(=O)C(C(c1ccccc1)N1CCOCC1)N1CCOCC1
折射率 1.55

 毒性和生态

 安全信息

海关编码 2934999090

 海关

海关编码 2934999090
中文概述 2934999090. 其他杂环化合物. 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
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 靶点实验

查看更多实验

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: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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 英文别名

3,4-dimorpholino-4-phenyl-butan-2-one
Morpholine,1-acetyl-2-(phenylethylene)di
3,4-Di-4-morpholinyl-4-phenyl-2-butanone
4-(2-Acetyl-2-morpholino-1-phenylethyl)morpholine
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