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2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚

更新时间:2025-08-26 00:16:21

2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式
2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式
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常用名 2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚 英文名 Phenol,2-methoxy-4-[(1E)-2-nitroethenyl]
CAS号 22568-51-0 分子量 195.17200
密度 1.308g/cm3 沸点 347ºC at 760mmHg
分子式 C9H9NO4 熔点 N/A
MSDS N/A 闪点 163.7ºC

 2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚名称

中文名 2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚
英文名 2-methoxy-4-(2-nitroethenyl)phenol

 2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚物理化学性质

密度 1.308g/cm3
沸点 347ºC at 760mmHg
分子式 C9H9NO4
分子量 195.17200
闪点 163.7ºC
精确质量 195.05300
PSA 75.28000
LogP 2.17140
InChIKey XVXCSPJSXIUNQJ-SNAWJCMRSA-N
SMILES COc1cc(C=C[N+](=O)[O-])ccc1O

 2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚合成线路

~89%

2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式

2-甲氧基-4-[(e)-2-...

22568-51-0

文献:Yang, Jianxin; Dong, Jing; Lue, Xia; Zhang, Qiang; Ding, Wei; Shi, Xiaoxin Chinese Journal of Chemistry, 2012 , vol. 30, # 12 p. 2827 - 2833

~82%

2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式

2-甲氧基-4-[(e)-2-...

22568-51-0

文献:Sridhar Rao; Srinivas; Suresh Babu; Madhusudana Rao Tetrahedron Letters, 2005 , vol. 46, # 47 p. 8141 - 8143

~60%

2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式

2-甲氧基-4-[(e)-2-...

22568-51-0

文献:Anuradha; Srinivas, Pullela V.; Ranga Rao; Manjulatha; Purohit, Muralidhar G.; Madhusudana Rao Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 20 p. 6820 - 6826

~8%

2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式

2-甲氧基-4-[(e)-2-...

22568-51-0

文献:Messere, Anna; Gentili, Alessandra; Garella, Isidoro; Temussi, Fabio; Di Blasio, Benedetto; Fiorentino, Antonio Synthetic Communications, 2004 , vol. 34, # 18 p. 3317 - 3324

~%

2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式

2-甲氧基-4-[(e)-2-...

22568-51-0

文献:Makarow Journal fuer Praktische Chemie (Leipzig), 1934 , vol. <2> 141, p. 77,89 Zhurnal Obshchei Khimii, 1935 , vol. 5, p. 39,47

~%

2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚结构式

2-甲氧基-4-[(e)-2-...

22568-51-0

文献:Armarego,W.L.F. Journal of the Chemical Society [Section] C: Organic, 1969 , p. 986 - 990

 2-甲氧基-4-[(e)-2-硝基乙烯基]苯酚靶点实验

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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
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:Inhibition of recombinant Syk
来源:ChEMBL
靶标:Tyrosine-protein kinase SYK
External Id:CHEMBL1022010
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: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
实验名称:HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules: Confir...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:N/A
External Id:HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules: Confirmation Assay, R21NS057026
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.
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
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