8-nitronaphthalen-1-amine结构式
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常用名 | 8-nitronaphthalen-1-amine | 英文名 | 8-nitronaphthalen-1-amine |
|---|---|---|---|---|
| CAS号 | 3229-89-8 | 分子量 | 188.18300 | |
| 密度 | 1.366g/cm3 | 沸点 | 385.3ºC at 760 mmHg | |
| 分子式 | C10H8N2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 186.8ºC |
| 英文名 | 8-nitronaphthalen-1-amine |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.366g/cm3 |
|---|---|
| 沸点 | 385.3ºC at 760 mmHg |
| 分子式 | C10H8N2O2 |
| 分子量 | 188.18300 |
| 闪点 | 186.8ºC |
| 精确质量 | 188.05900 |
| PSA | 71.84000 |
| LogP | 3.43460 |
| InChIKey | SOOKWSYBWVCXEB-UHFFFAOYSA-N |
| SMILES | Nc1cccc2cccc([N+](=O)[O-])c12 |
| 折射率 | 1.728 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):无 2.氢键供体数量:1 3.氢键受体数量:3 4.可旋转化学键数量:0 5.互变异构体数量:无 6.拓扑分子极性表面积:71.8 7.重原子数量:14 8.表面电荷:0 9.复杂度:227 10.同位素原子数量:0 11.确定原子立构中心数量:0 12.不确定原子立构中心数量:0 13.确定化学键立构中心数量:0 14.不确定化学键立构中心数量:0 15.共价键单元数量:1 |
| 海关编码 | 2921450090 |
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8-nitronaphthal... 3229-89-8 |
| 文献:Morgan; Micklethwait Journal of the Chemical Society, 1906 , vol. 89, p. 11 Full Text Show Details Meldola; Streatfeild Journal of the Chemical Society, 1893 , vol. 63, p. 1057 |
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8-nitronaphthal... 3229-89-8 |
| 文献:Vesely; Rein Collection of Czechoslovak Chemical Communications, vol. 1, p. 360 Chem. Zentralbl., 1929 , vol. 100, # II p. 1669 |
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8-nitronaphthal... 3229-89-8 |
| 文献:Hodgson; Davey Journal of the Chemical Society, 1939 , p. 348 |
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8-nitronaphthal... 3229-89-8 |
| 文献:Vesely; Rein Collection of Czechoslovak Chemical Communications, vol. 1, p. 364 Chem. Zentralbl., 1929 , vol. 100, # II p. 1669 |
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8-nitronaphthal... 3229-89-8
详细
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| 文献:Hodgson; Crook Journal of the Chemical Society, 1936 , p. 1844,1846 |
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详细
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| 文献:Meldola; Streatfeild Journal of the Chemical Society, 1893 , vol. 63, p. 1057 |
| 8-nitronaphthalen-1-amine上游产品 6 | |
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| 8-nitronaphthalen-1-amine下游产品 2 | |
| 海关编码 | 2921450090 |
|---|---|
| 中文概述 | 2921450090. 1-萘胺和2-萘胺的衍生物及盐(包括1-萘胺). 增值税率:17.0%. 退税率:9.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| Summary | 2921450090 1-naphthylamine (α-naphthylamine), 2-naphthylamine (β-naphthylamine) and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0% |
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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: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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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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| 8-nitro-1-naphthaleneamine |
| 8-nitronaphthylamine |
| 8-Nitro-1-amino-naphthalin |
| 8-nitro-1-naphthylamine |
| 1-amino-8-nitronaphthtalene |
| 1-amino-8-nitronaphthalene |