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Benzenamine,5-nitro-2-(phenylmethoxy)

更新时间:2026-02-11 18:44:24

Benzenamine,5-nitro-2-(phenylmethoxy)结构式
Benzenamine,5-nitro-2-(phenylmethoxy)结构式
品牌特惠专场
常用名 Benzenamine,5-nitro-2-(phenylmethoxy) 英文名 Benzenamine,5-nitro-2-(phenylmethoxy)
CAS号 88964-90-3 分子量 244.24600
密度 1.297g/cm3 沸点 453.9ºC at 760mmHg
分子式 C13H12N2O3 熔点 N/A
MSDS N/A 闪点 228.3ºC

 Benzenamine,5-nitro-2-(phenylmethoxy)名称

英文名 5-nitro-2-phenylmethoxyaniline
英文别名 更多

 Benzenamine,5-nitro-2-(phenylmethoxy)物理化学性质

密度 1.297g/cm3
沸点 453.9ºC at 760mmHg
分子式 C13H12N2O3
分子量 244.24600
闪点 228.3ºC
精确质量 244.08500
PSA 81.07000
LogP 3.86040
InChIKey VWLXPSZDHYNSRA-UHFFFAOYSA-N
SMILES Nc1cc([N+](=O)[O-])ccc1OCc1ccccc1
折射率 1.644

 Benzenamine,5-nitro-2-(phenylmethoxy)合成线路

 Benzenamine,5-nitro-2-(phenylmethoxy)靶点实验

查看更多实验

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: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
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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 Benzenamine,5-nitro-2-(phenylmethoxy)英文别名

2-Benzyloxy-5-nitro-anilin
5-nitro-2-benzyloxyaniline
2-amino-4-nitrophenyl benzyl ether
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