3-(4-氟苯基)-1-苯基-1H-吡唑-4-甲醛结构式
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常用名 | 3-(4-氟苯基)-1-苯基-1H-吡唑-4-甲醛 | 英文名 | 3-(4-FLUORO-PHENYL)-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE |
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| CAS号 | 36640-40-1 | 分子量 | 266.27000 | |
| 密度 | 1.2g/cm3 | 沸点 | 439.3ºC at 760 mmHg | |
| 分子式 | C16H11FN2O | 熔点 | 158-160℃ | |
| MSDS | N/A | 闪点 | 219.5ºC |
| 中文名 | 3-(4-氟-苯基)-1-苯基-1H-吡唑-4-甲醛 |
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| 英文名 | 3-(4-fluorophenyl)-1-phenylpyrazole-4-carbaldehyde |
| 中文别名 | 3-(4-氟苯基)-1-苯基-1H-吡唑-4-甲醛 |
| 英文别名 | 更多 |
| 密度 | 1.2g/cm3 |
|---|---|
| 沸点 | 439.3ºC at 760 mmHg |
| 熔点 | 158-160℃ |
| 分子式 | C16H11FN2O |
| 分子量 | 266.27000 |
| 闪点 | 219.5ºC |
| 精确质量 | 266.08600 |
| PSA | 34.89000 |
| LogP | 3.49090 |
| InChIKey | AQESLSBUZSGPEX-UHFFFAOYSA-N |
| SMILES | O=Cc1cn(-c2ccccc2)nc1-c1ccc(F)cc1 |
| 折射率 | 1.609 |
| 储存条件 | 2-8°C |
| 海关编码 | 2933199090 |
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| 3-(4-氟苯基)-1-苯基-1H-吡唑-4-甲醛上游产品 4 | |
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| 3-(4-氟苯基)-1-苯基-1H-吡唑-4-甲醛下游产品 4 | |
| 海关编码 | 2933199090 |
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| 中文概述 | 2933199090. 其他结构上有非稠合吡唑环化合物. 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:20.0% |
| 申报要素 | 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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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:Luminescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of ADP-glo R...
来源:Broad Institute
靶标:N/A
External Id:2046-03_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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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:Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Syn...
来源:Broad Institute
靶标:glycogen synthase kinase 3 beta isoform 1 [Homo sapiens]
External Id:2046-02_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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| 1-phenyl-3-(p-fluorophenyl)-pyrazol-4-aldehyde |
| 3-(4-Fluoro-phenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde |
| N-phenyl-3-p-fluorophenyl-4-formylpyrazole |
| 1-Phenyl-3-(p-fluor-phenyl)-pyrazol-4-aldehyd |