5-硝基-2-哌啶基吡啶结构式
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常用名 | 5-硝基-2-哌啶基吡啶 | 英文名 | 5-Nitro-2-(piperidine-1-yl)pyridine |
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| CAS号 | 26820-61-1 | 分子量 | 207.22900 | |
| 密度 | 1.242g/cm3 | 沸点 | 380.4ºC at 760mmHg | |
| 分子式 | C10H13N3O2 | 熔点 | 83-84 °C | |
| MSDS | N/A | 闪点 | 183.9ºC |
| 中文名 | 5-硝基-2-哌啶酮吡啶 |
|---|---|
| 英文名 | 5-nitro-2-piperidin-1-ylpyridine |
| 中文别名 | 5-硝基-2-哌啶基吡啶 |
| 英文别名 | 更多 |
| 密度 | 1.242g/cm3 |
|---|---|
| 沸点 | 380.4ºC at 760mmHg |
| 熔点 | 83-84 °C |
| 分子式 | C10H13N3O2 |
| 分子量 | 207.22900 |
| 闪点 | 183.9ºC |
| 精确质量 | 207.10100 |
| PSA | 61.95000 |
| LogP | 2.56830 |
| InChIKey | RQPFYHQIEVITPC-UHFFFAOYSA-N |
| SMILES | O=[N+]([O-])c1ccc(N2CCCCC2)nc1 |
| 蒸汽压 | 5.45E-06mmHg at 25°C |
| 折射率 | 1.582 |
| 储存条件 | 室温, 密封, 干燥 |
| 危害码 (欧洲) | Xn |
|---|---|
| 海关编码 | 2933990090 |
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~99%
5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Isanbor, Chukwuemeka; Emokpae, Thomas A. International Journal of Chemical Kinetics, 2008 , vol. 40, # 3 p. 125 - 135 |
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~95%
5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Gulevskaya, Anna V.; Maes, Bert U. W.; Meyers, Caroline; Herrebout, Wouter A.; Van Der Veken, Benjamin J. European Journal of Organic Chemistry, 2006 , # 23 p. 5305 - 5314 |
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~52%
5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Marcelis, Antonius T. M.; Plas, Henk C. van der Tetrahedron, 1989 , vol. 45, # 9 p. 2693 - 2702 |
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5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Morton-Norwich Products, Inc. Patent: US3947434 A1, 1976 ; |
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5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Mangini; Colonna Gazzetta Chimica Italiana, 1943 , vol. 73, p. 323,327 |
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~%
5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Isanbor, Chukwuemeka; Emokpae, Thomas A. International Journal of Chemical Kinetics, 2008 , vol. 40, # 3 p. 125 - 135 |
|
~%
5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Colonna; Dal Monte Casoni Bollettino Scientifico della Facolta di Chimica Industriale di Bologna, 1944 , vol. 5, p. 32 |
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~%
5-硝基-2-哌啶基吡啶 26820-61-1 |
| 文献:Yoneda Yakugaku Zasshi, 1957 , vol. 77, p. 944 Chem.Abstr., 1958 , p. 2855 |
| 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% |
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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: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
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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: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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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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实验名称:Confirmed inhibitors of the Choline Transporter (CHT)
来源:1043
靶标:high affinity choline transporter 1 [Homo sapiens]
External Id:SAID_488997
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实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
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| Piperidine,5-nitro-2-pyridyl |
| 5-nitro-2-piperidinopyridine |
| 5-nitro-2-piperidylpyridine |
| 2-piperidino-5-nitropyridine |