2-氨基-5-溴苯并恶唑结构式
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常用名 | 2-氨基-5-溴苯并恶唑 | 英文名 | 5-Bromo-1,3-benzoxazol-2-amine |
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| CAS号 | 64037-07-6 | 分子量 | 213.031 | |
| 密度 | 1.8±0.1 g/cm3 | 沸点 | 340.4±34.0 °C at 760 mmHg | |
| 分子式 | C7H5BrN2O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 159.7±25.7 °C |
| 中文名 | 5-溴苯[D]恶唑-2-胺 |
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| 英文名 | 5-bromo-1,3-benzoxazol-2-amine |
| 中文别名 | 2-氨基-5-溴苯并恶唑 | 5-溴苯并[d]噁唑-2-胺 | 5-溴-1,3-苯并恶唑-2-胺 |
| 英文别名 | 更多 |
| 密度 | 1.8±0.1 g/cm3 |
|---|---|
| 沸点 | 340.4±34.0 °C at 760 mmHg |
| 分子式 | C7H5BrN2O |
| 分子量 | 213.031 |
| 闪点 | 159.7±25.7 °C |
| 精确质量 | 211.958511 |
| PSA | 52.05000 |
| LogP | 2.64 |
| InChIKey | HMRSJGDFTOUVBW-UHFFFAOYSA-N |
| SMILES | Nc1nc2cc(Br)ccc2o1 |
| 蒸汽压 | 0.0±0.7 mmHg at 25°C |
| 折射率 | 1.716 |
| 储存条件 | 库房通风低温干燥 |
| 危害码 (欧洲) | Xi |
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| 海关编码 | 2934999090 |
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2-氨基-5-溴苯并恶唑 64037-07-6 |
| 文献:INTELLIKINE, LLC; REN, Pingda; MARTIN, Michael Patent: WO2013/23184 A1, 2013 ; Location in patent: Paragraph 00231; 00232 ; WO 2013/023184 A1 |
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2-氨基-5-溴苯并恶唑 64037-07-6 |
| 文献:WO2010/51042 A1, ; Page/Page column 133 ; |
| 2-氨基-5-溴苯并恶唑上游产品 2 | |
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| 2-氨基-5-溴苯并恶唑下游产品 4 | |
| 海关编码 | 2934999090 |
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| 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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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: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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| 2-Amino-5-brom-benzoxazol |
| 5-bromobenzo[d]oxazol-2-amine |
| 5-Brom-2-amino-benzoxazol |
| 2-Benzoxazolamine,5-bromo |
| 5-Bromo-1,3-benzoxazol-2-amine |
| BENZOXAZOLE,2-AMINO-5-BROMO |
| 2-Amino-5-bromobenzoxazole |
| 5-bromo-benzooxazol-2-ylamine |