N-(pyrrol-2-ylidenemethyl)aniline

• 常用名: N-(pyrrol-2-ylidenemethyl)aniline
• 英文名: N-(pyrrol-2-ylidenemethyl)aniline
• CAS号: 4089-09-2
• 分子量: 170.21000
• 密度: 1.05g/cm3
• 沸点: 291.5ºC at 760 mmHg
• 分子式: C₁₁H₁₀N₂
• 熔点: N/A
• 闪点: 130.1ºC

N-(pyrrol-2-ylidenemethyl)aniline名称

• 英文名: N-(pyrrol-2-ylidenemethyl)aniline

N-(pyrrol-2-ylidenemethyl)aniline物理化学性质

• 密度: 1.05g/cm3
• 沸点: 291.5ºC at 760 mmHg
• 分子式: C₁₁H₁₀N₂
• 分子量: 170.21000
• 闪点: 130.1ºC
• 精确质量: 170.08400
• PSA: 28.15000
• LogP: 2.76530
• InChIKey: XDLMLLMWCIBZIU-UHFFFAOYSA-N
• SMILES: C(=Nc1ccccc1)c1ccc[nH]1
• 折射率: 1.584

N-(pyrrol-2-ylidenemethyl)aniline安全信息

• 海关编码: 2933990090

N-(pyrrol-2-ylidenemethyl)aniline海关

• 海关编码: 2933990090
• 中文概述: 2933990090. 其他仅含氮杂原子的杂环化合物. 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: 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

N-(pyrrol-2-ylidenemethyl)aniline靶点实验

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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

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

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

实验名称：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1100

实验名称：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1101

实验名称：Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas... 来源：Broad Institute 靶标：N/A External Id：2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2

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

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

实验名称：High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce... 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School 靶标：N/A External Id：HMS1149-MLP

实验名称：qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima... 来源：NCGC 靶标：apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7] External Id：AMA1100

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N-(pyrrol-2-ylidenemethyl)aniline英文别名

• N-(2-pyrrolidene)aniline
• N-(pyrrolyl-2-methylene)aniline
• phenyl(1H-pyrrole-2-ylmethylene)amine
• N-Pyrrolylmethylene aniline
• phenyl(1H-pyrrol-2-ylmethylene)amine
• pyrrol-2-ylmethylenephenylamine
• 2-pyrrolecarbaldmethylimine