1,4-哌嗪二乙胺结构式
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常用名 | 1,4-哌嗪二乙胺 | 英文名 | Piperazine-1,4-diethylamine |
|---|---|---|---|---|
| CAS号 | 6531-38-0 | 分子量 | 172.271 | |
| 密度 | 1.0±0.1 g/cm3 | 沸点 | 302.2±10.0 °C at 760 mmHg | |
| 分子式 | C8H20N4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 151.4±7.0 °C |
| 中文名 | N,N'-二(氨乙基)-哌嗪 |
|---|---|
| 英文名 | 2-[4-(2-aminoethyl)piperazin-1-yl]ethanamine |
| 中文别名 | N,N'-二(2-氨乙基)-哌嗪,1,4-哌嗪二乙胺 | 1,4-哌嗪二乙胺 | N,N'-二(2氨乙基)-哌嗪 |
| 英文别名 | 更多 |
| 密度 | 1.0±0.1 g/cm3 |
|---|---|
| 沸点 | 302.2±10.0 °C at 760 mmHg |
| 分子式 | C8H20N4 |
| 分子量 | 172.271 |
| 闪点 | 151.4±7.0 °C |
| 精确质量 | 172.168793 |
| PSA | 58.52000 |
| LogP | -1.97 |
| InChIKey | PAOXFRSJRCGJLV-UHFFFAOYSA-N |
| SMILES | NCCN1CCN(CCN)CC1 |
| 蒸汽压 | 0.0±0.6 mmHg at 25°C |
| 折射率 | 1.512 |
| 危险品运输编码 | UN 1760 |
|---|---|
| 包装等级 | II |
| 海关编码 | 2933599090 |
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~87%
1,4-哌嗪二乙胺 6531-38-0 |
| 文献:Filosa, Rosanna; Peduto, Antonella; Micco, Simone Di; Caprariis, Paolo de; Festa, Michela; Petrella, Antonello; Capranico, Giovanni; Bifulco, Giuseppe Bioorganic and Medicinal Chemistry, 2009 , vol. 17, # 1 p. 13 - 24 |
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~%
1,4-哌嗪二乙胺 6531-38-0 |
| 文献:European Journal of Organic Chemistry, , # 6 p. 1050 - 1055 |
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~81%
1,4-哌嗪二乙胺 6531-38-0 |
| 文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 58, # 9 p. 2098 - 2102,1868 - 1871 |
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~%
1,4-哌嗪二乙胺 6531-38-0 |
| 文献:Journal of Organic Chemistry USSR (English Translation), , vol. 23, p. 330 - 332 Zhurnal Organicheskoi Khimii, , vol. 23, # 2 p. 370 - 372 |
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~75%
1,4-哌嗪二乙胺 6531-38-0 |
| 文献:Ganin, E.V.; Makarov, V.F.; Nikitin, V.I. Journal of Organic Chemistry USSR (English Translation), 1987 , vol. 23, p. 330 - 332 Zhurnal Organicheskoi Khimii, 1987 , vol. 23, # 2 p. 370 - 372 |
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~%
1,4-哌嗪二乙胺 6531-38-0 |
| 文献:Journal of Organic Chemistry USSR (English Translation), , vol. 23, p. 330 - 332 Zhurnal Organicheskoi Khimii, , vol. 23, # 2 p. 370 - 372 |
| 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% |
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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
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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
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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
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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
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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
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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
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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
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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.
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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
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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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| 2-[4-(2-Amino-ethyl)-piperazin-1-yl]-ethylamine |
| 2,2'-(1,4-Piperazinediyl)diethanamine |
| 1,4-Piperazinediethanamine |
| Piperazine-1,4-diethylamine |
| 2,2'-piperazine-1,4-diyldiethanamine |