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3-(4-苯基-1-哌嗪)-1-丙胺

更新时间:2025-08-29 13:43:39

3-(4-苯基-1-哌嗪)-1-丙胺结构式
3-(4-苯基-1-哌嗪)-1-丙胺结构式
品牌特惠专场
常用名 3-(4-苯基-1-哌嗪)-1-丙胺 英文名 3-(4-Phenylpiperazin-1-yl)propan-1-amine
CAS号 20529-19-5 分子量 219.32600
密度 1.041g/cm3 沸点 355.3ºC at 760 mmHg
分子式 C13H21N3 熔点 N/A
MSDS N/A 闪点 166.2ºC

 3-(4-苯基-1-哌嗪)-1-丙胺名称

中文名 3-(4-苯基-1-哌嗪)-1-丙胺
英文名 3-(4-Phenylpiperazin-1-yl)propan-1-amine
英文别名 更多

 3-(4-苯基-1-哌嗪)-1-丙胺物理化学性质

密度 1.041g/cm3
沸点 355.3ºC at 760 mmHg
分子式 C13H21N3
分子量 219.32600
闪点 166.2ºC
精确质量 219.17400
PSA 32.50000
LogP 1.86060
InChIKey KNLCRNWJXCLJHQ-UHFFFAOYSA-N
SMILES NCCCN1CCN(c2ccccc2)CC1
蒸汽压 3.15E-05mmHg at 25°C
折射率 1.554

 3-(4-苯基-1-哌嗪)-1-丙胺安全信息

海关编码 2933599090

 3-(4-苯基-1-哌嗪)-1-丙胺合成线路

~72%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Biswas, Swati; Zhang, Suhong; Fernandez, Fernando; Ghosh, Balaram; Zhen, Juan; Kuzhikandathil, Eldo; Reith, Maarten E. A.; Dutta, Aloke K. Journal of Medicinal Chemistry, 2008 , vol. 51, # 1 p. 101 - 117

~72%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Nagarapu, Lingaiah; Mateti, Jhansi; Gaikwad, Hanmant K.; Bantu, Rajashaker; Sheeba Rani; Prameela Subhashini Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21, # 14 p. 4138 - 4140

~%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Bioorganic and Medicinal Chemistry, , vol. 14, # 22 p. 7539 - 7550

~54%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Synaptic Pharmaceutical Corporation Patent: US5767131 A1, 1998 ;

~%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Bioorganic and Medicinal Chemistry, , vol. 6, # 6 p. 849 - 868

~%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Bioorganic and Medicinal Chemistry Letters, , vol. 7, # 18 p. 2399 - 2402

~%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Yakugaku Zasshi, , vol. 76, p. 644,647, 648 Chem.Abstr., , p. 425

~%

3-(4-苯基-1-哌嗪)-1-丙胺结构式

3-(4-苯基-1-哌嗪)-1-丙胺

20529-19-5

文献:Yakugaku Zasshi, , vol. 76, p. 644,647, 648 Chem.Abstr., , p. 425

 3-(4-苯基-1-哌嗪)-1-丙胺海关

海关编码 2933599090
中文概述 2933599090. 其他结构上有嘧啶环的化合物(包括其他结构上有哌嗪环的化合物. 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 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 3-(4-苯基-1-哌嗪)-1-丙胺靶点实验

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:qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
来源:NCGC
External Id:tdp43-p2-repeat
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 3-(4-苯基-1-哌嗪)-1-丙胺英文别名

3-(4-phenylpiperzin-1-yl)propan-1-amine
1-piperazinepropanamine,4-phenyl
4-(phenyl)-1-piperazinepropanamine
2-(4-phenylpiperazine)propylamine
1-(3-amino-1-propyl)-4-phenylpiperazine
N'-phenyl-N-(3-aminopropyl)-piperazine
1-phenyl-4-(3-aminopropyl)-piperazine
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