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4-(吡咯烷-1-基)吡啶-2-甲酸

更新时间:2025-08-26 00:00:54

4-(吡咯烷-1-基)吡啶-2-甲酸结构式
4-(吡咯烷-1-基)吡啶-2-甲酸结构式
品牌特惠专场
常用名 4-(吡咯烷-1-基)吡啶-2-甲酸 英文名 2-Pyridinecarboxylicacid, 4-(1-pyrrolidinyl)
CAS号 66933-69-5 分子量 192.21400
密度 1.283g/cm3 沸点 416.1ºC at 760mmHg
分子式 C10H12N2O2 熔点 N/A
MSDS N/A 闪点 205.5ºC

 4-(吡咯烷-1-基)吡啶-2-甲酸名称

中文名 4-吡咯烷基-1-吡啶-2-羧酸盐酸盐
英文名 4-pyrrolidin-1-ylpyridine-2-carboxylic acid
英文别名 更多

 4-(吡咯烷-1-基)吡啶-2-甲酸物理化学性质

密度 1.283g/cm3
沸点 416.1ºC at 760mmHg
分子式 C10H12N2O2
分子量 192.21400
闪点 205.5ºC
精确质量 192.09000
PSA 53.43000
LogP 1.44500
InChIKey BFBSDJMGXPOZJS-UHFFFAOYSA-N
SMILES O=C(O)c1cc(N2CCCC2)ccn1
折射率 1.603
储存条件 室温, 密封, 干燥

 4-(吡咯烷-1-基)吡啶-2-甲酸安全信息

海关编码 2933990090

 4-(吡咯烷-1-基)吡啶-2-甲酸合成线路

~%

4-(吡咯烷-1-基)吡啶-2-甲酸结构式

4-(吡咯烷-1-基)吡啶-2-甲酸

66933-69-5

文献:Wieprecht, Torsten; Schlingloff, Gunther; Xia, Juntao; Heinz, Uwe; Schneider, Abert; Dubs, Marie-Josee; Bachmann, Frank; Hazekamp, Menno; Dannacher, Josef Patent: US2006/19853 A1, 2006 ; Location in patent: Page/Page column 20 ;

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4-(吡咯烷-1-基)吡啶-2-甲酸结构式

4-(吡咯烷-1-基)吡啶-2-甲酸

66933-69-5

文献:Bogdanowicz, Agnieszka; Foks, Henryk; Gobis, Katarzyna; Augustynowicz-Kopec, Ewa Heteroatom Chemistry, 2012 , vol. 23, # 2 p. 223 - 230

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4-(吡咯烷-1-基)吡啶-2-甲酸结构式

4-(吡咯烷-1-基)吡啶-2-甲酸

66933-69-5

文献:Bogdanowicz, Agnieszka; Foks, Henryk; Gobis, Katarzyna; Augustynowicz-Kopec, Ewa Heteroatom Chemistry, 2012 , vol. 23, # 2 p. 223 - 230

 4-(吡咯烷-1-基)吡啶-2-甲酸上下游产品

4-(吡咯烷-1-基)吡啶-2-甲酸上游产品  4

4-(吡咯烷-1-基)吡啶-2-甲酸下游产品  0

 4-(吡咯烷-1-基)吡啶-2-甲酸海关

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%

 4-(吡咯烷-1-基)吡啶-2-甲酸靶点实验

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: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
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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 4-(吡咯烷-1-基)吡啶-2-甲酸英文别名

4-(pyrrolidin-1-yl)picolinic acid
4-(1-Pyrrolidinyl)picolinsaeure
4-pyrrolidin-1-yl-pyridine-2-carboxylic acid
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