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N-苄基-1-氮杂双环[2.2.2]-3-辛胺

更新时间:2025-08-30 09:33:09

N-苄基-1-氮杂双环[2.2.2]-3-辛胺结构式
N-苄基-1-氮杂双环[2.2.2]-3-辛胺结构式
品牌特惠专场
常用名 N-苄基-1-氮杂双环[2.2.2]-3-辛胺 英文名 1-Azabicyclo[2.2.2]octan-3-amine,N-(phenylmethyl)
CAS号 6530-11-6 分子量 216.32200
密度 1.08g/cm3 沸点 327.7ºC at 760mmHg
分子式 C14H20N2 熔点 N/A
MSDS N/A 闪点 134.9ºC

 N-苄基-1-氮杂双环[2.2.2]-3-辛胺名称

中文名 N-苄基-1-氮杂双环[2.2.2]-3-辛胺
英文名 N-benzyl-1-azabicyclo[2.2.2]octan-3-amine
英文别名 更多

 N-苄基-1-氮杂双环[2.2.2]-3-辛胺物理化学性质

密度 1.08g/cm3
沸点 327.7ºC at 760mmHg
分子式 C14H20N2
分子量 216.32200
闪点 134.9ºC
精确质量 216.16300
PSA 15.27000
LogP 2.19920
InChIKey BMCRQEPTJNQZST-UHFFFAOYSA-N
SMILES c1ccc(CNC2CN3CCC2CC3)cc1
折射率 1.588

 N-苄基-1-氮杂双环[2.2.2]-3-辛胺安全信息

海关编码 2933990090

 N-苄基-1-氮杂双环[2.2.2]-3-辛胺合成线路

~76%

N-苄基-1-氮杂双环[2.2.2]-3-辛胺结构式

N-苄基-1-氮杂双环[2.2...

6530-11-6

文献:JANSSEN PHARMACEUTICA, N.V. Patent: WO2004/35574 A2, 2004 ; Location in patent: Page 30 ; WO 2004/035574 A2

~%

N-苄基-1-氮杂双环[2.2.2]-3-辛胺结构式

N-苄基-1-氮杂双环[2.2...

6530-11-6

文献:Delalande S.A. Patent: US4657911 A1, 1987 ;

 N-苄基-1-氮杂双环[2.2.2]-3-辛胺上下游产品

N-苄基-1-氮杂双环[2.2.2]-3-辛胺上游产品  3

N-苄基-1-氮杂双环[2.2.2]-3-辛胺下游产品  0

 N-苄基-1-氮杂双环[2.2.2]-3-辛胺海关

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%

 N-苄基-1-氮杂双环[2.2.2]-3-辛胺靶点实验

查看更多实验

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: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
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
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
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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
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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 N-苄基-1-氮杂双环[2.2.2]-3-辛胺英文别名

(1-aza-bicyclo[2.2.2]oct-3-yl)-benzyl-amine
3-Benzylaminochinuclidin
N-(phenylmethyl)-1-azabicyclo[2.2.2]octan-3-amine
3-(Benzylamino)quinuclidine
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