2-(1-苄基-4-哌啶基)-2-氰基乙酸乙酯结构式
|
常用名 | 2-(1-苄基-4-哌啶基)-2-氰基乙酸乙酯 | 英文名 | ethyl 2-(1-benzylpiperidin-4-ylidene)-2-cyanoacetate |
|---|---|---|---|---|
| CAS号 | 1463-52-1 | 分子量 | 284.35300 | |
| 密度 | 1.148g/cm3 | 沸点 | 430.4ºC at 760mmHg | |
| 分子式 | C17H20N2O2 | 熔点 | 64-67ºC | |
| MSDS | N/A | 闪点 | 214.1ºC |
| 中文名 | 2-(1-苄基-4-哌啶基)-2-氰基乙酸乙酯 |
|---|---|
| 英文名 | ethyl 2-(1-benzylpiperidin-4-ylidene)-2-cyanoacetate |
| 英文别名 | 更多 |
| 密度 | 1.148g/cm3 |
|---|---|
| 沸点 | 430.4ºC at 760mmHg |
| 熔点 | 64-67ºC |
| 分子式 | C17H20N2O2 |
| 分子量 | 284.35300 |
| 闪点 | 214.1ºC |
| 精确质量 | 284.15200 |
| PSA | 53.33000 |
| LogP | 2.60358 |
| InChIKey | HSTSIRUENGPGSB-UHFFFAOYSA-N |
| SMILES | CCOC(=O)C(C#N)=C1CCN(Cc2ccccc2)CC1 |
| 蒸汽压 | 1.31E-07mmHg at 25°C |
| 折射率 | 1.561 |
| 海关编码 | 2933399090 |
|---|
|
~99%
2-(1-苄基-4-哌啶基)-... 1463-52-1 |
| 文献:NOVARTIS AG; NOVARTIS PHARMA GMBH Patent: WO2004/69256 A1, 2004 ; Location in patent: Page/Page column 41 ; WO 2004/069256 A1 |
|
~85%
2-(1-苄基-4-哌啶基)-... 1463-52-1 |
| 文献:Asadipour, Ali; Alipour, Masoumeh; Jafari, Mona; Khoobi, Mehdi; Emami, Saeed; Nadri, Hamid; Sakhteman, Amirhossein; Moradi, Alireza; Sheibani, Vahid; Homayouni Moghadam, Farshad; Shafiee, Abbas; Foroumadi, Alireza European Journal of Medicinal Chemistry, 2013 , vol. 70, p. 623 - 630 |
|
~%
2-(1-苄基-4-哌啶基)-... 1463-52-1 |
| 文献:European Journal of Medicinal Chemistry, , vol. 70, p. 623 - 630 |
| 2-(1-苄基-4-哌啶基)-2-氰基乙酸乙酯上游产品 4 | |
|---|---|
| 2-(1-苄基-4-哌啶基)-2-氰基乙酸乙酯下游产品 10 | |
| 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% |
|
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
|
|
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: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
|
|
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
|
|
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:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
|
|
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
|
| (1-Benzyl-[4]piperidyliden)-cyan-essigsaeure-aethylester |
| (1-benzylpiperidin-4-ylidine)cyanoacetic acid ethyl ester |
| ethyl 2-cyano-2-[1-(phenylmethyl)-4-piperidinylidene]acetate |
| (1-benzyl-piperidin-4-ylidene)-cyano-acetic acid ethyl ester |
| ethyl (1-benzyl-4-piperidylidene)cyanoacetate |
| ethyl 2-(1-benzyl-4-piperidinylidene)-2-cyanoacetate |