3-(4-甲氧基苯基)-2-苯基丙酸结构式
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常用名 | 3-(4-甲氧基苯基)-2-苯基丙酸 | 英文名 | Benzenepropanoic acid,4-methoxy-a-phenyl |
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| CAS号 | 4314-68-5 | 分子量 | 256.29600 | |
| 密度 | 1.171g/cm3 | 沸点 | 381.2ºC at 760mmHg | |
| 分子式 | C16H16O3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 138ºC |
| 中文名 | 3-(4-甲氧基苯基)-2-苯基丙酸 |
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| 英文名 | 3-(4-methoxyphenyl)-2-phenylpropanoic acid |
| 中文别名 | 3-(4-甲氧基苯基)-2-苯丙酸 |
| 英文别名 | 更多 |
| 密度 | 1.171g/cm3 |
|---|---|
| 沸点 | 381.2ºC at 760mmHg |
| 分子式 | C16H16O3 |
| 分子量 | 256.29600 |
| 闪点 | 138ºC |
| 精确质量 | 256.11000 |
| PSA | 46.53000 |
| LogP | 3.10610 |
| InChIKey | GIROORGDVPRQFZ-UHFFFAOYSA-N |
| SMILES | COc1ccc(CC(C(=O)O)c2ccccc2)cc1 |
| 储存条件 | 避光,通风干燥处,密封保存 |
| 稳定性 | 常温常压下稳定 |
| 分子结构 | 1、 摩尔折射率:73.16 2、 摩尔体积(m3/mol):218.8 3、 等张比容(90.2K):572.9 4、 表面张力(dyne/cm):46.9 5、 极化率(10 -24cm 3):29.00 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):3.3 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:5 5.互变异构体数量:无 6.拓扑分子极性表面积46.5 7.重原子数量:19 8.表面电荷:0 9.复杂度:276 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:粉末 2. 密度(g/mL):不确定 3. 相对蒸汽密度(g/mL,空气=1):不确定 4. 熔点(ºC):不确定 5. 沸点(ºC,常压):不确定 6. 沸点(ºC, 16mmHg):不确定 7. 折射率:不确定 8. 闪点(ºC):不确定 9. 比旋光度(º, C=4, H2O):不确定 10. 自燃点或引燃温度(ºC):不确定 11. 蒸气压(kPa,25ºC):不确定 12. 饱和蒸气压(kPa,60ºC):不确定 13. 燃烧热(KJ/mol):不确定 14. 临界温度(ºC):不确定 15. 临界压力(KPa):不确定 16. 油水(辛醇/水)分配系数的对数值:不确定 17. 爆炸上限(%,V/V):不确定 18. 爆炸下限(%,V/V):不确定 19. 溶解性:不确定 |
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3-(4-甲氧基苯基)-2-苯基丙酸毒理学数据: 主要的刺激性影响 在皮肤上面:刺激皮肤和粘膜 在眼睛上面:刺激的影响 过敏作用:没有已知的敏化影响 3-(4-甲氧基苯基)-2-苯基丙酸生态学数据: 该物质对环境可能有危害,对水体应给予特别注意 |
| 危害码 (欧洲) | Xi: Irritant; |
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| 海关编码 | 2918990090 |
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~97%
3-(4-甲氧基苯基)-2-苯基丙酸 4314-68-5 |
| 文献:ORION CORPORATION Patent: WO2004/63191 A1, 2004 ; Location in patent: Page 45-46 ; |
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~%
3-(4-甲氧基苯基)-2-苯基丙酸 4314-68-5 |
| 文献:Szllsi, Gyoergy; Herman, Beata; Szabados, Erika; Fueloep, Ferenc; Bartok, Mihaly Journal of Molecular Catalysis A: Chemical, 2010 , vol. 333, # 1-2 p. 28 - 36 |
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~%
3-(4-甲氧基苯基)-2-苯基丙酸 4314-68-5 |
| 文献:Szllsi, Gyoergy; Herman, Beata; Szabados, Erika; Fueloep, Ferenc; Bartok, Mihaly Journal of Molecular Catalysis A: Chemical, 2010 , vol. 333, # 1-2 p. 28 - 36 |
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~%
3-(4-甲氧基苯基)-2-苯基丙酸 4314-68-5 |
| 文献:Lednicer,D. et al. Journal of Medicinal Chemistry, 1965 , vol. 8, p. 52 - 57 |
| 3-(4-甲氧基苯基)-2-苯基丙酸上游产品 3 | |
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| 3-(4-甲氧基苯基)-2-苯基丙酸下游产品 1 | |
| 海关编码 | 2918990090 |
|---|---|
| 中文概述 | 2918990090. 其他含其他附加含氧基羧酸(包括酸酐、酰卤化物、过氧化物和过氧酸及该税号的衍生物). 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:30.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| Summary | 2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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实验名称:A screen for compounds that inhibit cell wall-associated teichoic acid synthesis in S...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS704
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实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
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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:Agonist activity at human N-terminal His6-tagged PDK1 amino acid residues 51 to 359 e...
来源:ChEMBL
靶标:3-phosphoinositide-dependent protein kinase 1
External Id:CHEMBL2343759
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
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实验名称:Dissociation constant for HCV NS3 protease substrate binding site
来源:ChEMBL
靶标:Genome polyprotein
External Id:CHEMBL751815
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实验名称:NCI human tumor cell line growth inhibition assay. Data for the MCF7 Non-Small Cell L...
来源:DTP/NCI
靶标:N/A
External Id:MCF7_OneDose
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实验名称:Inhibition constant for HCV NS3 protease substrate binding site; ND=Not determined
来源:ChEMBL
靶标:Genome polyprotein
External Id:CHEMBL751818
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| f9995-0092 |