2-氨基-6-氯苯并恶唑

• 常用名: 2-氨基-6-氯苯并恶唑
• 英文名: 2-Amino-6-chlorobenzoxazole
• CAS号: 52112-68-2
• 分子量: 168.58000
• 密度: 1.481g/cm3
• 沸点: 316.8ºC at 760 mmHg
• 分子式: C₇H₅ClN₂O
• 熔点: N/A
• 闪点: 145.4ºC

2-氨基-6-氯苯并恶唑名称

• 中文名: 2-氨基-6-氯苯并噁唑
• 英文名: 2-Amino-6-chlorobenzoxazole
• 中文别名: 2-氨基-6-氯苯并恶唑

2-氨基-6-氯苯并恶唑物理化学性质

• 密度: 1.481g/cm3
• 沸点: 316.8ºC at 760 mmHg
• 分子式: C₇H₅ClN₂O
• 分子量: 168.58000
• 闪点: 145.4ºC
• 精确质量: 168.00900
• PSA: 52.05000
• LogP: 2.64460
• InChIKey: QDMXVLGVKMTTIT-UHFFFAOYSA-N
• SMILES: Nc1nc2ccc(Cl)cc2o1
• 折射率: 1.692
• 储存条件: 库房通风低温干燥

2-氨基-6-氯苯并恶唑MSDS

2-氨基-6-氯苯并恶唑MSDS英文版

2-氨基-6-氯苯并恶唑毒性和生态

2-氨基-6-氯苯并恶唑安全信息

• 危害码 (欧洲): Xi
• 海关编码: 2934999090

2-氨基-6-氯苯并恶唑海关

• 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%

2-氨基-6-氯苯并恶唑靶点实验

查看更多实验

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

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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2-氨基-6-氯苯并恶唑英文别名

• 6-chloro-1,3-benzoxazol-2-amine
• 6-Chlorobenzo[d]oxazol-2-amine