4-(2-四氢-1H-吡咯-1-基乙基)吡啶结构式
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常用名 | 4-(2-四氢-1H-吡咯-1-基乙基)吡啶 | 英文名 | 4-(2-pyrrolidin-1-ylethyl)pyridine |
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| CAS号 | 67580-65-8 | 分子量 | 176.25800 | |
| 密度 | 1.029g/cm3 | 沸点 | 120-124ºC 4mm | |
| 分子式 | C11H16N2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 121.6ºC |
| 中文名 | 4-(吡咯烷基乙酯)哌啶 |
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| 英文名 | 4-(2-pyrrolidin-1-ylethyl)pyridine |
| 中文别名 | 4-吡咯啉基乙基吡啶 | 4-(2-四氢-1H-吡咯-1-乙基)吡啶 |
| 英文别名 | 更多 |
| 密度 | 1.029g/cm3 |
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| 沸点 | 120-124ºC 4mm |
| 分子式 | C11H16N2 |
| 分子量 | 176.25800 |
| 闪点 | 121.6ºC |
| 精确质量 | 176.13100 |
| PSA | 16.13000 |
| LogP | 1.65780 |
| InChIKey | GNJYGFKCUMGKOY-UHFFFAOYSA-N |
| SMILES | c1cc(CCN2CCCC2)ccn1 |
| 折射率 | 1.542 |
| 分子结构 | 1、 摩尔折射率:53.91 2、 摩尔体积(m3/mol):171.2 3、 等张比容(90.2K):436.4 4、 表面张力(dyne/cm):42.1 5、 极化率(10 -24cm 3):21.37 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):1.6 2.氢键供体数量:0 3.氢键受体数量:2 4.可旋转化学键数量:3 5.互变异构体数量:无 6.拓扑分子极性表面积16.1 7.重原子数量:13 8.表面电荷:0 9.复杂度:135 10.同位素原子数量:0 11.确定原子立构中心数量:0 12.不确定原子立构中心数量:0 13.确定化学键立构中心数量:0 14.不确定化学键立构中心数量:0 15.共价键单元数量:1 |
| 更多 | 1. 性状:。 2. 密度(g/mL,25/4℃):未确定 3. 相对蒸汽密度(g/mL,空气=1):未确定 4. 熔点(ºC):未确定 5. 沸点(ºC,常压):未确定 6. 沸点(ºC,5.2kPa):未确定 7. 折射率:未确定 8. 闪点(ºC):未确定 9. 比旋光度(º):未确定 10. 自燃点或引燃温度(ºC):未确定 11. 蒸气压(kPa,25ºC):未确定 12. 饱和蒸气压(kPa,60ºC):未确定 13. 燃烧热(KJ/mol):未确定 14. 临界温度(ºC):未确定 15. 临界压力(KPa):未确定 16. 油水(辛醇/水)分配系数的对数值:未确定 17. 爆炸上限(%,V/V):未确定 18. 爆炸下限(%,V/V):未确定 19. 溶解性:。 |
| 危害码 (欧洲) | C |
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| 海关编码 | 2933990090 |
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4-(2-四氢-1H-吡咯-1... 67580-65-8 |
| 文献:Journal of the American Chemical Society, , vol. 78, p. 4441 Journal of the American Chemical Society, , vol. 78, p. 4127,4129 Journal fuer Praktische Chemie (Leipzig), , vol. <4> 4, p. 19,20 |
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4-(2-四氢-1H-吡咯-1... 67580-65-8 |
| 文献:Bioorganic and Medicinal Chemistry Letters, , vol. 18, # 1 p. 355 - 359 |
| 4-(2-四氢-1H-吡咯-1-基乙基)吡啶上游产品 2 | |
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| 4-(2-四氢-1H-吡咯-1-基乙基)吡啶下游产品 1 | |
| 海关编码 | 2933990090 |
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| 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: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: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: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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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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| 4-(2-(Pyrrolidin-1-yl)-ethyl)-pyridin |
| 4-(2-Pyrrolidino-aethyl)-pyridin |
| 4-(2-Tetrahydro-1H-pyrrol-1-ylethyl)pyridine |
| 4-(2-pyrrolidino-ethyl)-pyridine |
| 4-[2-(pyrrolidin-1-yl)ethyl]pyridine |