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2-氨基-5-溴苯并恶唑

更新时间:2025-08-25 18:41:27

2-氨基-5-溴苯并恶唑结构式
2-氨基-5-溴苯并恶唑结构式
品牌特惠专场
常用名 2-氨基-5-溴苯并恶唑 英文名 5-Bromo-1,3-benzoxazol-2-amine
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

 2-氨基-5-溴苯并恶唑名称

中文名 5-溴苯[D]恶唑-2-胺
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

 2-氨基-5-溴苯并恶唑物理化学性质

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

 2-氨基-5-溴苯并恶唑毒性和生态

 2-氨基-5-溴苯并恶唑安全信息

危害码 (欧洲) Xi
海关编码 2934999090

 2-氨基-5-溴苯并恶唑合成线路

~97%

2-氨基-5-溴苯并恶唑结构式

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

~%

2-氨基-5-溴苯并恶唑结构式

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-5-溴苯并恶唑靶点实验

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-5-溴苯并恶唑英文别名

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
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