N-benzothiazol-2-yl-N-phenyl-acetamide结构式
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常用名 | N-benzothiazol-2-yl-N-phenyl-acetamide | 英文名 | N-benzothiazol-2-yl-N-phenyl-acetamide |
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| CAS号 | 5401-29-6 | 分子量 | 268.33400 | |
| 密度 | 1.312g/cm3 | 沸点 | 411.3ºC at 760 mmHg | |
| 分子式 | C15H12N2OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 202.5ºC |
| 英文名 | N-(1,3-benzothiazol-2-yl)-N-phenylacetamide |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.312g/cm3 |
|---|---|
| 沸点 | 411.3ºC at 760 mmHg |
| 分子式 | C15H12N2OS |
| 分子量 | 268.33400 |
| 闪点 | 202.5ºC |
| 精确质量 | 268.06700 |
| PSA | 61.44000 |
| LogP | 3.98090 |
| InChIKey | CZXGMKQRPSDFMP-UHFFFAOYSA-N |
| SMILES | CC(=O)N(c1ccccc1)c1nc2ccccc2s1 |
| 折射率 | 1.703 |
| 海关编码 | 2934999090 |
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N-benzothiazol-... 5401-29-6 |
| 文献:Dyson; Hunter; Soyka Journal of the Chemical Society, 1929 , p. 464 |
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N-benzothiazol-... 5401-29-6 |
| 文献:Jacobson; Frankenbacher Chemische Berichte, 1891 , vol. 24, p. 1408 Full Text Show Details Hugershoff Chemische Berichte, 1903 , vol. 36, p. 3128 Chemische Berichte, 1901 , vol. 34, p. 3136 |
|
~%
N-benzothiazol-... 5401-29-6 |
| 文献:Jacobson; Frankenbacher Chemische Berichte, 1891 , vol. 24, p. 1408 Full Text Show Details Hugershoff Chemische Berichte, 1903 , vol. 36, p. 3128 Chemische Berichte, 1901 , vol. 34, p. 3136 |
| N-benzothiazol-2-yl-N-phenyl-acetamide上游产品 3 | |
|---|---|
| N-benzothiazol-2-yl-N-phenyl-acetamide下游产品 0 | |
| 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% |
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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
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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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| N-benzothiazol-2-yl-N-phenyl-acetamide |
| HMS3078I15 |