5-硝基咪唑-4-甲酸甲酯结构式
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常用名 | 5-硝基咪唑-4-甲酸甲酯 | 英文名 | 1H-Imidazole-4-carboxylicacid, 5-nitro-, methyl ester |
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| CAS号 | 20271-20-9 | 分子量 | 171.11100 | |
| 密度 | 1.545g/cm3 | 沸点 | 409.7ºC at 760mmHg | |
| 分子式 | C5H5N3O4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 201.6ºC |
| 中文名 | 5-硝基咪唑-4-甲酸甲酯 |
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| 英文名 | methyl 4-nitro-1H-imidazole-5-carboxylate |
| 英文别名 | 更多 |
| 密度 | 1.545g/cm3 |
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| 沸点 | 409.7ºC at 760mmHg |
| 分子式 | C5H5N3O4 |
| 分子量 | 171.11100 |
| 闪点 | 201.6ºC |
| 精确质量 | 171.02800 |
| PSA | 100.80000 |
| LogP | 0.62770 |
| InChIKey | YGTWILAKCGDEML-UHFFFAOYSA-N |
| SMILES | COC(=O)c1nc[nH]c1[N+](=O)[O-] |
| 蒸汽压 | 6.38E-07mmHg at 25°C |
| 折射率 | 1.584 |
| 储存条件 | 室温,干燥 |
| 海关编码 | 2933290090 |
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~45%
5-硝基咪唑-4-甲酸甲酯 20271-20-9 |
| 文献:MERCK SHARP and DOHME LIMITED; HOLLINGWORTH, Gregory, John; JONES, A., Brian; SPAREY, Timothy, Jason Patent: WO2005/49613 A1, 2005 ; Location in patent: Page/Page column 44 ; WO 2005/049613 A1 |
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~%
5-硝基咪唑-4-甲酸甲酯 20271-20-9 |
| 文献:Windaus; Langenbeck Chemische Berichte, 1923 , vol. 56, p. 684 |
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~%
5-硝基咪唑-4-甲酸甲酯 20271-20-9 |
| 文献:Kulew; Roshkow Zhurnal Obshchei Khimii, 1957 , vol. 27, p. 1389;engl.Ausg.S.1470 |
| 5-硝基咪唑-4-甲酸甲酯上游产品 3 | |
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| 5-硝基咪唑-4-甲酸甲酯下游产品 3 | |
| 海关编码 | 2933290090 |
|---|---|
| 中文概述 | 2933290090. 其他结构含非稠合咪唑环的化合物. 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 | 2933290090. other compounds containing an unfused imidazole 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: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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| Imidazole-4-carboxylic acid,5-nitro-,methyl ester |
| methyl 5-nitroimidazole-4-carboxylate |
| methyl-5-nitro-4-imidazolecarboxylate |
| 5-Nitro-1(3)H-imidazol-4-carbonsaeure-methylester |
| 5-nitro-1(3)H-imidazole-4-carboxylic acid methyl ester |
| 5-nitro-imidazole-4-carboxylic acid methyl ester |
| Methyl 5-nitro-1H-imidazole-4-carboxylate |
| 1H-Imidazole-4-carboxylic acid,5-nitro-,methyl ester |
| 5-Imidazolic acid,4-nitro-,methyl ester |