Benzamide, 4-methoxy-N-2-propen-1-yl结构式
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常用名 | Benzamide, 4-methoxy-N-2-propen-1-yl | 英文名 | Benzamide, 4-methoxy-N-2-propen-1-yl |
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| CAS号 | 66897-25-4 | 分子量 | 191.22600 | |
| 密度 | 1.051g/cm3 | 沸点 | 348.9ºC at 760mmHg | |
| 分子式 | C11H13NO2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 164.8ºC |
| 英文名 | 4-methoxy-N-prop-2-enylbenzamide |
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| 英文别名 | 更多 |
| 密度 | 1.051g/cm3 |
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| 沸点 | 348.9ºC at 760mmHg |
| 分子式 | C11H13NO2 |
| 分子量 | 191.22600 |
| 闪点 | 164.8ºC |
| 精确质量 | 191.09500 |
| PSA | 38.33000 |
| LogP | 2.00190 |
| InChIKey | JZNQXUMFZGPDMF-UHFFFAOYSA-N |
| SMILES | C=CCNC(=O)c1ccc(OC)cc1 |
| 折射率 | 1.522 |
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~90%
Benzamide, 4-me... 66897-25-4 |
| 文献:Harvey, Daniel F.; Sigano, Dina M. Journal of Organic Chemistry, 1996 , vol. 61, # 7 p. 2268 - 2272 |
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~79%
Benzamide, 4-me... 66897-25-4 |
| 文献:Baburajan, Poongavanam; Elango, Kuppanagounder P. Tetrahedron Letters, 2014 , vol. 55, # 5 p. 1006 - 1010 |
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~79%
Benzamide, 4-me... 66897-25-4 |
| 文献:Appukkuttan, Prasad; Axelsson, Linda; der Eycken, Erik Van; Larhed, Mats Tetrahedron Letters, 2008 , vol. 49, # 39 p. 5625 - 5628 |
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~%
Benzamide, 4-me... 66897-25-4 |
| 文献:Cline, Gary W.; Hanna, Samir B. Journal of Organic Chemistry, 1988 , vol. 53, # 15 p. 3583 - 3586 |
| Benzamide, 4-methoxy-N-2-propen-1-yl上游产品 4 | |
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| Benzamide, 4-methoxy-N-2-propen-1-yl下游产品 2 | |
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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: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: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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