4-戊基苯乙酸结构式
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常用名 | 4-戊基苯乙酸 | 英文名 | 4-Pentylphenyl acetic acid |
|---|---|---|---|---|
| CAS号 | 14377-21-0 | 分子量 | 206.28100 | |
| 密度 | 1.035g/cm3 | 沸点 | 333.6ºC at 760mmHg | |
| 分子式 | C13H18O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 230.7ºC |
| 中文名 | 4-戊基苯乙酸 |
|---|---|
| 英文名 | 2-(4-pentylphenyl)acetic acid |
| 英文别名 | 更多 |
| 密度 | 1.035g/cm3 |
|---|---|
| 沸点 | 333.6ºC at 760mmHg |
| 分子式 | C13H18O2 |
| 分子量 | 206.28100 |
| 闪点 | 230.7ºC |
| 精确质量 | 206.13100 |
| PSA | 37.30000 |
| LogP | 3.04640 |
| InChIKey | YAAVVJAWWNQMCY-UHFFFAOYSA-N |
| SMILES | CCCCCc1ccc(CC(=O)O)cc1 |
| 蒸汽压 | 5.34E-05mmHg at 25°C |
| 折射率 | 1.522 |
| 储存条件 | 室温,干燥 |
| 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:2 4.可旋转化学键数量:6 5.互变异构体数量:无 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:181 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 |
| 危害码 (欧洲) | Xi |
|---|---|
| 海关编码 | 2916399090 |
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4-戊基苯乙酸 14377-21-0 |
| 文献:Molecular crystals and liquid crystals, , vol. 97, # 1-4 p. 13 - 28 |
|
~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Molecular crystals and liquid crystals, , vol. 97, # 1-4 p. 13 - 28 |
|
~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Molecular crystals and liquid crystals, , vol. 97, # 1-4 p. 13 - 28 |
|
~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Molecular crystals and liquid crystals, , vol. 97, # 1-4 p. 13 - 28 |
|
~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Molecular crystals and liquid crystals, , vol. 97, # 1-4 p. 13 - 28 |
|
~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Tetrahedron, , vol. 23, p. 1735 - 1738 |
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~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Tetrahedron, , vol. 23, p. 1735 - 1738 |
|
~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Tetrahedron, , vol. 23, p. 1735 - 1738 |
|
~%
4-戊基苯乙酸 14377-21-0 |
| 文献:Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), , # 4 p. 1159 - 1160 |
| 海关编码 | 2916399090 |
|---|---|
| 中文概述 | 2916399090 其他芳香一元羧酸. 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, 丙烯酸、丙烯酸盐或酯应报明包装 |
| Summary | 2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% 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: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: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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