7-氯萘-2-醇结构式
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常用名 | 7-氯萘-2-醇 | 英文名 | 7-chloronaphthalen-2-ol |
|---|---|---|---|---|
| CAS号 | 40492-93-1 | 分子量 | 178.61500 | |
| 密度 | 1.333g/cm3 | 沸点 | 331.9ºC at 760 mmHg | |
| 分子式 | C10H7ClO | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 154.5ºC |
| 中文名 | 7-氯萘-2-醇 |
|---|---|
| 英文名 | 7-chloronaphthalen-2-ol |
| 英文别名 | 更多 |
| 密度 | 1.333g/cm3 |
|---|---|
| 沸点 | 331.9ºC at 760 mmHg |
| 分子式 | C10H7ClO |
| 分子量 | 178.61500 |
| 闪点 | 154.5ºC |
| 精确质量 | 178.01900 |
| PSA | 20.23000 |
| LogP | 3.19880 |
| InChIKey | QSDSWPOSISCSSI-UHFFFAOYSA-N |
| SMILES | Oc1ccc2ccc(Cl)cc2c1 |
| 外观性状 | 淡黄色粉末 |
| 折射率 | 1.684 |
| 储存条件 | 室温, 密封, 干燥, 惰性气体 |
| 危害码 (欧洲) | Xn |
|---|
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7-氯萘-2-醇 40492-93-1 |
| 文献:Rosowsky; Battaglia; Chen; Papathanasopoulos; Modest Journal of the Chemical Society. Perkin transactions 1, 1969 , vol. 10, p. 1376 - 1378 |
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7-氯萘-2-醇 40492-93-1 |
| 文献:Rosowsky; Battaglia; Chen; Papathanasopoulos; Modest Journal of the Chemical Society. Perkin transactions 1, 1969 , vol. 10, p. 1376 - 1378 |
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7-氯萘-2-醇 40492-93-1 |
| 文献:James; Woodcock Journal of the Chemical Society, 1951 , p. 3418,3419 |
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7-氯萘-2-醇 40492-93-1 |
| 文献:James; Woodcock Journal of the Chemical Society, 1951 , p. 3418,3419 |
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7-氯萘-2-醇 40492-93-1 |
| 文献:Franzen; Deibel Journal fuer Praktische Chemie (Leipzig), 1908 , vol. <2> 78, p. 153 |
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External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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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
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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: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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实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
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External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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| 7-chloro-2-naphthalenol |
| 7-Chlor-2-hydroxy-naphthalin |
| 2-Naphthalenol,7-chloro |
| 7-Chlor-[2]naphthol |
| 2-Chloro-7-hydroxynaphthalene |
| 7-Chlor-naphthol-(2) |
| 7-Chloro-2-naphthol |