3-羟基-1H-PHENALEN-1-酮结构式
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常用名 | 3-羟基-1H-PHENALEN-1-酮 | 英文名 | 3-Hydroxy-1H-phenalen-1-one |
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| CAS号 | 5472-84-4 | 分子量 | 196.201 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | 407.3±45.0 °C at 760 mmHg | |
| 分子式 | C13H8O2 | 熔点 | 264ºC(lit.) | |
| MSDS | N/A | 闪点 | 173.9±21.3 °C |
| 中文名 | 3-羟基-1H-PHENALEN-1-酮 |
|---|---|
| 英文名 | 3-hydroxyphenalen-1-one |
| 中文别名 | 3-羟基-1H-非那烯-1-酮 |
| 英文别名 | 更多 |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 沸点 | 407.3±45.0 °C at 760 mmHg |
| 熔点 | 264ºC(lit.) |
| 分子式 | C13H8O2 |
| 分子量 | 196.201 |
| 闪点 | 173.9±21.3 °C |
| 精确质量 | 196.052429 |
| PSA | 37.30000 |
| LogP | 3.21 |
| InChIKey | DXBYIIARRIMNFJ-UHFFFAOYSA-N |
| SMILES | O=C1C=C(O)c2cccc3cccc1c23 |
| 蒸汽压 | 0.0±1.0 mmHg at 25°C |
| 折射率 | 1.779 |
| 储存条件 | 密封储存,储存于阴凉、干燥的库房。 |
| 稳定性 | 避免与不相容材料接触。与强氧化剂反应。 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):2.5 2.氢键供体数量:1 3.氢键受体数量:2 4.可旋转化学键数量:0 5.互变异构体数量:2 6.拓扑分子极性表面积37.3 7.重原子数量:15 8.表面电荷:0 9.复杂度:319 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 |
| 更多 | 1. 性状:黄绿色粉末 2. 密度(g/mL,25℃):未确定 3. 相对蒸汽密度(g/mL,空气=1):未确定 4. 熔点(ºC):264 5. 沸点(ºC,常压):未确定 6. 沸点(ºC,0.5mmHg):未确定 7. 折射率(n20/D):未确定 8. 闪点(ºC):未确定 9. 比旋光度(º):未确定 10. 自燃点或引燃温度(ºC):未确定 11. 蒸气压(mmHg,20ºC):未确定 12. 饱和蒸气压(kPa,25ºC):未确定 13. 燃烧热(KJ/mol):未确定 14. 临界温度(ºC):未确定 15. 临界压力(KPa):未确定 16. 油水(辛醇/水)分配系数的对数值:未确定 17. 爆炸上限(%,V/V):未确定 18. 爆炸下限(%,V/V):未确定 19. 溶解性:未确定 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:Gazzetta Chimica Italiana, , vol. 41 I, p. 191 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:Journal of the American Chemical Society, , vol. 73, p. 1230 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:Chemische Berichte, , vol. 71, p. 1102,1114 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:DE753210 , ; DRP/DRBP Org.Chem. |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:Chemische Berichte, , vol. 102, # 6 p. 1988 - 2002 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:DE283365 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 12, p. 496 Chemische Berichte, , vol. 55, p. 3289 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:Chemische Berichte, , vol. 102, # 6 p. 1988 - 2002 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:Chemische Berichte, , vol. 101, # 6 p. 2162 - 2175 |
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3-羟基-1H-PHENALEN-1-酮 5472-84-4 |
| 文献:Chemische Berichte, , vol. 55, p. 3289 |
| 3-羟基-1H-PHENALEN-1-酮上游产品 9 | |
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| 3-羟基-1H-PHENALEN-1-酮下游产品 9 | |
| 海关编码 | 2914400090 |
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| 中文概述 | 2914400090 其他酮醇及酮醛。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:5.5%。普通关税:30.0% |
| 申报要素 | 品名, 成分含量, 用途, 丙酮报明包装 |
| Summary | 2914400090 other ketone-alcohols and ketone-aldehydes。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0% |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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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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| 4-hydroxy-1H-phenalen-1-one |
| 3-hydroxy-phenalen-1-one |
| 3-Hydroxy-phenalen-1-on |
| 3-Hydroxy-1H-phenalen-1-one |
| 3-hydroxy-1H-phenalene-1-one |
| 3-hydroxyperinaphthenone |
| MFCD00029247 |