N-(吡啶-2-基)苯甲酰胺结构式
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常用名 | N-(吡啶-2-基)苯甲酰胺 | 英文名 | N-(Pyridin-2-yl)benzamide |
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| CAS号 | 4589-12-2 | 分子量 | 198.22100 | |
| 密度 | 1.227g/cm3 | 沸点 | 265.8ºC at 760 mmHg | |
| 分子式 | C12H10N2O | 熔点 | 114.5 °C | |
| MSDS | N/A | 闪点 | 114.5ºC |
| 中文名 | N-(吡啶-2-基)苯甲酰胺 |
|---|---|
| 英文名 | N-pyridin-2-ylbenzamide |
| 英文别名 | 更多 |
| 密度 | 1.227g/cm3 |
|---|---|
| 沸点 | 265.8ºC at 760 mmHg |
| 熔点 | 114.5 °C |
| 分子式 | C12H10N2O |
| 分子量 | 198.22100 |
| 闪点 | 114.5ºC |
| 精确质量 | 198.07900 |
| PSA | 41.99000 |
| LogP | 2.40690 |
| InChIKey | LZIJKEIPCFEOLH-UHFFFAOYSA-N |
| SMILES | O=C(Nc1ccccn1)c1ccccc1 |
| 折射率 | 1.65 |
| 储存条件 | 2-8°C |
| 海关编码 | 2933399090 |
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| N-(吡啶-2-基)苯甲酰胺上游产品 10 | |
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| N-(吡啶-2-基)苯甲酰胺下游产品 3 | |
| 海关编码 | 2933399090 |
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| 中文概述 | 2933399090. 其他结构含非稠合吡啶环的化合物. 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 | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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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:Selectivity index, ratio of IC50 for HEK293 cells to IC50 for Trypanosoma brucei bruc...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL3371076
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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:Antimicrobial activity against bloodstream form of Trypanosoma brucei brucei 427 afte...
来源:ChEMBL
靶标:Trypanosoma brucei brucei
External Id:CHEMBL3371074
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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: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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| N-(pyridin-2-yl)benzamide |
| Benzamide,N-2-pyridinyl |
| N-(2-pyridinyl)benzamide |
| F3332-0073 |
| 2-(benzoylamino)pyridine |
| N-pyridin-2-ylbenzamine |
| N-(pyrid-2-yl)benzamide |