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1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛

更新时间:2025-08-23 23:41:02

1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛结构式
1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛结构式
品牌特惠专场
常用名 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛 英文名 1-(4-METHOXYPHENYL)-1H-PYRROLE-2-CARBALDEHYDE
CAS号 30186-36-8 分子量 201.22100
密度 1.1g/cm3 沸点 347.1ºC at 760 mmHg
分子式 C12H11NO2 熔点 N/A
MSDS N/A 闪点 163.7ºC

 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛名称

中文名 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛
英文名 1-(4-methoxyphenyl)pyrrole-2-carbaldehyde
中文别名 1-(4-甲氧基苯)-1H-吡咯-2-甲醛
英文别名 更多

 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛物理化学性质

密度 1.1g/cm3
沸点 347.1ºC at 760 mmHg
分子式 C12H11NO2
分子量 201.22100
闪点 163.7ºC
精确质量 201.07900
PSA 31.23000
LogP 2.29840
InChIKey VBOUNTHJXKGWSS-UHFFFAOYSA-N
SMILES COc1ccc(-n2cccc2C=O)cc1
折射率 1.557

 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛安全信息

危害码 (欧洲) Xi
海关编码 2933990090

 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛合成线路

~83%

1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛结构式

1-(4-甲氧基-苯基)-1H...

30186-36-8

文献:Dumoulin, H.; Rault, S.; Robba, M. Journal of Heterocyclic Chemistry, 1995 , vol. 32, # 6 p. 1703 - 1707

~14%

1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛结构式

1-(4-甲氧基-苯基)-1H...

30186-36-8

文献:Pina, M. del' K.; Budylin, V. A.; Rodriges, M.; Terent'ev, P. B.; Bundel', Yu. G. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1989 , vol. 25, # 2 p. 142 - 146 Khimiya Geterotsiklicheskikh Soedinenii, 1989 , vol. 25, # 2 p. 180 - 184

~%

1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛结构式

1-(4-甲氧基-苯基)-1H...

30186-36-8

文献:Dumoulin, H.; Rault, S.; Robba, M. Journal of Heterocyclic Chemistry, 1995 , vol. 32, # 6 p. 1703 - 1707

 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛海关

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%

 1-(4-甲氧基-苯基)-1H-吡咯-2-甲醛靶点实验

查看更多实验

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: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: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
实验名称:qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
来源:NCGC
External Id:tdp43-p2-repeat
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-(4-甲氧基-苯基)-1H-吡咯-2-甲醛英文别名

N-(4-methoxyphenyl)pyrrole-2-carboxaldehyde
1-(4-methoxyphenyl)-1H-pyrrole-2-carbaldehyde
HMS2567P15
1-(p-Methoxyphenyl)-2-pyrrolcarboxaldehyd
1-(4-methoxy-phenyl)-pyrrole-2-carbaldehyde
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