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3-(1H-吡咯-1-基)苯胺

更新时间:2025-08-27 12:03:38

3-(1H-吡咯-1-基)苯胺结构式
3-(1H-吡咯-1-基)苯胺结构式
品牌特惠专场
常用名 3-(1H-吡咯-1-基)苯胺 英文名 3-(1H-Pyrrol-1-yl)aniline
CAS号 89353-42-4 分子量 158.200
密度 1.1±0.1 g/cm3 沸点 323.4±25.0 °C at 760 mmHg
分子式 C10H10N2 熔点 43-44ºC
MSDS N/A 闪点 149.4±23.2 °C

 3-(1H-吡咯-1-基)苯胺名称

中文名 3-(1H-吡咯-1-基)苯胺
英文名 3-pyrrol-1-ylaniline
英文别名 更多

 3-(1H-吡咯-1-基)苯胺物理化学性质

密度 1.1±0.1 g/cm3
沸点 323.4±25.0 °C at 760 mmHg
熔点 43-44ºC
分子式 C10H10N2
分子量 158.200
闪点 149.4±23.2 °C
精确质量 158.084396
PSA 30.95000
LogP 1.80
InChIKey PJGDCPOPSNUYHC-UHFFFAOYSA-N
SMILES Nc1cccc(-n2cccc2)c1
蒸汽压 0.0±0.7 mmHg at 25°C
折射率 1.602

 3-(1H-吡咯-1-基)苯胺MSDS

 3-(1H-吡咯-1-基)苯胺安全信息

危害码 (欧洲) Xi: Irritant;
风险声明 (欧洲) R36/37/38
安全声明 (欧洲) 26-36/37/39-37/39
海关编码 2933990090

 3-(1H-吡咯-1-基)苯胺合成线路

~64%

3-(1H-吡咯-1-基)苯胺结构式

3-(1H-吡咯-1-基)苯胺

89353-42-4

文献:Zhang, Xingxian; Shi, Junchen Tetrahedron, 2011 , vol. 67, # 5 p. 898 - 903

~89%

3-(1H-吡咯-1-基)苯胺结构式

3-(1H-吡咯-1-基)苯胺

89353-42-4

文献:Ma, Heng-Chang; Jiang, Xuan-Zhen Journal of Organic Chemistry, 2007 , vol. 72, # 23 p. 8943 - 8946

~49%

3-(1H-吡咯-1-基)苯胺结构式

3-(1H-吡咯-1-基)苯胺

89353-42-4

文献:Corelli; Massa; Stefancich; Artico; Panico; Simonetti Farmaco, Edizione Scientifica, 1984 , vol. 39, # 2 p. 95 - 109

~%

3-(1H-吡咯-1-基)苯胺结构式

3-(1H-吡咯-1-基)苯胺

89353-42-4

文献:Farmaco, Edizione Scientifica, , vol. 39, # 2 p. 95 - 109

~27%

3-(1H-吡咯-1-基)苯胺结构式

3-(1H-吡咯-1-基)苯胺

89353-42-4

文献:Asian Journal of Chemistry, , vol. 25, # 1 p. 501 - 504

 3-(1H-吡咯-1-基)苯胺海关

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%

 3-(1H-吡咯-1-基)苯胺靶点实验

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:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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: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
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 3-(1H-吡咯-1-基)苯胺英文别名

MFCD03407309
3-(1-pyrrolyl)aniline
1-(3-aminophenyl)pyrrole
1-(3-aminophenyl)-1H-pyrrole
3-(pyrrol-1-yl)aniline
3-(1H-Pyrrol-1-yl)aniline
3-pyrrolylphenylamine
3-Pyrrol-1-yl-phenylamine
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