3,4,6-三甲氧基-1(3H)-异苯并呋喃酮结构式
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常用名 | 3,4,6-三甲氧基-1(3H)-异苯并呋喃酮 | 英文名 | 3,4,6-trimethoxy-3H-2-benzofuran-1-one |
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| CAS号 | 189454-29-3 | 分子量 | 224.21000 | |
| 密度 | 1.28g/cm3 | 沸点 | 394.2ºC at 760 mmHg | |
| 分子式 | C11H12O5 | 熔点 | 149-152ºC(lit.) | |
| MSDS | N/A | 闪点 | 178.4ºC |
| 中文名 | 3,4,6-三甲氧基-1(3H)-异苯并呋喃酮 |
|---|---|
| 英文名 | 3,4,6-trimethoxy-3H-2-benzofuran-1-one |
| 中文别名 | ,4,6-三甲氧基-1(3H)-异苯并呋喃酮 | 3,4,6-三甲氧基苯酞 |
| 英文别名 | 更多 |
| 密度 | 1.28g/cm3 |
|---|---|
| 沸点 | 394.2ºC at 760 mmHg |
| 熔点 | 149-152ºC(lit.) |
| 分子式 | C11H12O5 |
| 分子量 | 224.21000 |
| 闪点 | 178.4ºC |
| 精确质量 | 224.06800 |
| PSA | 53.99000 |
| LogP | 1.51920 |
| InChIKey | JNVLFUCEKYADLU-UHFFFAOYSA-N |
| SMILES | COc1cc(OC)c2c(c1)C(=O)OC2OC |
| 蒸汽压 | 2.02E-06mmHg at 25°C |
| 折射率 | 1.54 |
| 储存条件 | 密封储存,储存于阴凉、干燥的库房。 |
| 稳定性 | 避免与强氧化剂接触。 |
| 分子结构 | 1、 疏水参数计算参考值(XlogP):1.3 2、 氢键供体数量:0 3、 氢键受体数量:5 4、 可旋转化学键数量:3 5、 互变异构体数量: 6、 拓扑分子极性表面积(TPSA):54 7、 重原子数量:16 8、 表面电荷:0 9、 复杂度:267 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:1 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 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):1.3 2.氢键供体数量:0 3.氢键受体数量:5 4.可旋转化学键数量:3 5.互变异构体数量:无 6.拓扑分子极性表面积54 7.重原子数量:16 8.表面电荷:0 9.复杂度:267 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:1 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:未确定 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):149-152 5. 沸点(ºC,常压):未确定 6. 沸点(ºC,0.2mmHg):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,217ºC):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 |
| WGK德国 | 3 |
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~95%
3,4,6-三甲氧基-1(3H... 189454-29-3 |
| 文献:Murty; Hazra; Datta; Mal Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1997 , vol. 36, # 2 p. 126 - 132 |
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3,4,6-三甲氧基-1(3H... 189454-29-3
详细
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| 文献:Ren, Jie; Jiang, Ju-Xing; Li, Ang-Bo; Liao, Tou-Geng; Tian, Ren-Rong; Chen, Xu-Lin; Jiang, Si-Ping; Pittman Jr., Charles U.; Zhu, Hua-Jie European Journal of Organic Chemistry, 2009 , # 23 p. 3987 - 3991 |
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~%
3,4,6-三甲氧基-1(3H... 189454-29-3 |
| 文献:Murty; Hazra; Datta; Mal Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1997 , vol. 36, # 2 p. 126 - 132 |
| 3,4,6-三甲氧基-1(3H)-异苯并呋喃酮上游产品 3 | |
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| 3,4,6-三甲氧基-1(3H)-异苯并呋喃酮下游产品 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:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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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:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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| 3,4,6-trimethoxy-1,3-dihydro-1-isobenzofuranone |
| MFCD01312574 |
| 3,4,6-Trimethoxy-1(3H)-isobenzofuranone |
| 3,4,6-trimethoxyphthalide |
| JNVLFUCEKYADLU-UHFFFAOYSA |
| 3,5,7-Trimethoxyphthalid |
| 3,4,6-trimethoxy-3H-isobenzofuran-1-one |