4-甲基-2,6-二氧代-4-苯基-3,5-哌啶二甲腈结构式
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常用名 | 4-甲基-2,6-二氧代-4-苯基-3,5-哌啶二甲腈 | 英文名 | 4-methyl-2,6-dioxo-4-phenyl-piperidine-3,5-dicarbonitrile |
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| CAS号 | 6936-95-4 | 分子量 | 253.25600 | |
| 密度 | 1.3g/cm3 | 沸点 | 566.5ºC at 760 mmHg | |
| 分子式 | C14H11N3O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 296.4ºC |
| 中文名 | 4-甲基-2,6-二氧代-4-苯基-3,5-哌啶二甲腈 |
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| 英文名 | 4-methyl-2,6-dioxo-4-phenylpiperidine-3,5-dicarbonitrile |
| 英文别名 | 更多 |
| 密度 | 1.3g/cm3 |
|---|---|
| 沸点 | 566.5ºC at 760 mmHg |
| 分子式 | C14H11N3O2 |
| 分子量 | 253.25600 |
| 闪点 | 296.4ºC |
| 精确质量 | 253.08500 |
| PSA | 93.75000 |
| LogP | 1.20906 |
| InChIKey | DUHIKGWFSCWEBA-UHFFFAOYSA-N |
| SMILES | CC1(c2ccccc2)C(C#N)C(=O)NC(=O)C1C#N |
| 折射率 | 1.591 |
| 海关编码 | 2926909090 |
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~74%
4-甲基-2,6-二氧代-4-... 6936-95-4 |
| 文献:Wu, Liqiang; Yang, Chunguang; Yang, Liming; Yang, Lijuan Heterocycles, 2009 , vol. 78, # 4 p. 977 - 982 |
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~%
4-甲基-2,6-二氧代-4-... 6936-95-4 |
| 文献:McElvain; Clemens Journal of the American Chemical Society, 1958 , vol. 80, p. 3915,3919 Organic Syntheses, 1963 , vol. Coll. Vol. IV, p. 662 |
| 4-甲基-2,6-二氧代-4-苯基-3,5-哌啶二甲腈上游产品 4 | |
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| 4-甲基-2,6-二氧代-4-苯基-3,5-哌啶二甲腈下游产品 0 | |
| 海关编码 | 2926909090 |
|---|---|
| 中文概述 | 2926909090 其他腈基化合物. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:6.5% 普通关税:30.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| Summary | HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |
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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: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
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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
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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
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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: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
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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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