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1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺

更新时间:2025-09-03 11:33:09

1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺结构式
1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺结构式
委托求购
常用名 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺 英文名 4-Piperidinecarboxamide,4-(ethylamino)-1-(phenylmethyl)
CAS号 1027-91-4 分子量 261.36300
密度 1.11g/cm3 沸点 432.8ºC at 760mmHg
分子式 C15H23N3O 熔点 N/A
MSDS N/A 闪点 215.5ºC

 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺名称

中文名 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺
英文名 1-benzyl-4-(ethylamino)piperidine-4-carboxamide
中文别名 1-苄基-4-(乙基氨基)哌啶-4-羧酰胺
英文别名 更多

 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺物理化学性质

密度 1.11g/cm3
沸点 432.8ºC at 760mmHg
分子式 C15H23N3O
分子量 261.36300
闪点 215.5ºC
精确质量 261.18400
PSA 58.36000
LogP 2.14510
InChIKey LPPPBYXGXSHYQJ-UHFFFAOYSA-N
SMILES CCNC1(C(N)=O)CCN(Cc2ccccc2)CC1
蒸汽压 1.08E-07mmHg at 25°C
折射率 1.577

 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺安全信息

海关编码 2933399090

 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺合成线路

~96%

1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺结构式

1-苯甲基-4-(乙胺基)哌啶...

1027-91-4

文献:TANABE SEIYAKU CO., LTD. Patent: WO2007/46550 A1, 2007 ; Location in patent: Page/Page column 127-128 ; WO 2007/046550 A1

 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺上下游产品

1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺上游产品  1

1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺下游产品  1

 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺海关

海关编码 2933399090
中文概述 2933399090. 其他结构含非稠合吡啶环的化合物. 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 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺靶点实验

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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 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺英文别名

1-Benzyl-4-ethylamino-4-carbamoyl-piperidin
HMS3085D05
1-Benzyl-4-carbamoyl-4-ethylamino-piperidin
1-benzyl-4-carbamoyl-4-(ethylamino)piperidine
1-benzyl-4-ethylamino-piperidine-4-carboxylic acid amide
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