5-甲氧基苯并[d]恶唑-2-胺

• 常用名: 5-甲氧基苯并[d]恶唑-2-胺
• 英文名: 5-Methoxy-1,3-benzoxazol-2-amine
• CAS号: 64037-14-5
• 分子量: 164.161
• 密度: 1.3±0.1 g/cm3
• 沸点: 320.2±34.0 °C at 760 mmHg
• 分子式: C₈H₈N₂O₂
• 熔点: N/A
• 闪点: 147.5±25.7 °C

5-甲氧基苯并[d]恶唑-2-胺名称

• 中文名: 5-甲氧基苯并[d]恶唑-2-胺
• 英文名: 5-methoxy-1,3-benzoxazol-2-amine

5-甲氧基苯并[d]恶唑-2-胺物理化学性质

• 密度: 1.3±0.1 g/cm3
• 沸点: 320.2±34.0 °C at 760 mmHg
• 分子式: C₈H₈N₂O₂
• 分子量: 164.161
• 闪点: 147.5±25.7 °C
• 精确质量: 164.058578
• PSA: 61.28000
• LogP: 1.78
• InChIKey: YCBIFQTZAQVLTQ-UHFFFAOYSA-N
• SMILES: COc1ccc2oc(N)nc2c1
• 外观性状: 固体
• 蒸汽压: 0.0±0.7 mmHg at 25°C
• 折射率: 1.641
• 储存条件: 库房通风低温干燥

5-甲氧基苯并[d]恶唑-2-胺毒性和生态

5-甲氧基苯并[d]恶唑-2-胺安全信息

• 危害码 (欧洲): Xn
• 海关编码: 2934999090

5-甲氧基苯并[d]恶唑-2-胺海关

• 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%

5-甲氧基苯并[d]恶唑-2-胺靶点实验

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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

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

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

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

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

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

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

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

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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5-甲氧基苯并[d]恶唑-2-胺英文别名

• BENZOXAZOLE,2-AMINO-5-METHOXY
• 2-Benzoxazolamine,5-methoxy
• 5-methoxy-benzooxazol-2-ylamine
• 2-Amino-5-methoxybenzoxazole
• 2-Amino-4-methoxy-benzoxazole
• HMS3093P03
• 5-Methoxy-1,3-benzoxazol-2-amine