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2-(2-呋喃基)-4-喹啉羧酸

更新时间:2025-08-25 09:29:36

2-(2-呋喃基)-4-喹啉羧酸结构式
2-(2-呋喃基)-4-喹啉羧酸结构式
品牌特惠专场
常用名 2-(2-呋喃基)-4-喹啉羧酸 英文名 2-(2-Furyl)-4-quinolinecarboxylic acid
CAS号 20146-25-2 分子量 239.22600
密度 1.348g/cm3 沸点 433.7ºC at 760mmHg
分子式 C14H9NO3 熔点 N/A
MSDS N/A 闪点 216.1ºC

 2-(2-呋喃基)-4-喹啉羧酸名称

中文名 2-(2-呋喃基)-4-喹啉羧酸
英文名 2-(2-Furyl)-4-quinolinecarboxylic acid
英文别名 更多

 2-(2-呋喃基)-4-喹啉羧酸物理化学性质

密度 1.348g/cm3
沸点 433.7ºC at 760mmHg
分子式 C14H9NO3
分子量 239.22600
闪点 216.1ºC
精确质量 239.05800
PSA 63.33000
LogP 3.19300
InChIKey WWEKTFINADFAEC-UHFFFAOYSA-N
SMILES O=C(O)c1cc(-c2ccco2)nc2ccccc12
蒸汽压 2.73E-08mmHg at 25°C
折射率 1.666

 2-(2-呋喃基)-4-喹啉羧酸安全信息

危害码 (欧洲) Xi
海关编码 2934999090

 2-(2-呋喃基)-4-喹啉羧酸合成线路

~73%

2-(2-呋喃基)-4-喹啉羧酸结构式

2-(2-呋喃基)-4-喹啉羧酸

20146-25-2

文献:Holla, B. Shivarama; Shridhara; Rao, B. Sooryanarayana; Poojary, K. Narayana Bollettino Chimico Farmaceutico, 2002 , vol. 141, # 2 p. 105 - 109

~%

2-(2-呋喃基)-4-喹啉羧酸结构式

2-(2-呋喃基)-4-喹啉羧酸

20146-25-2

文献:Bioorganic and Medicinal Chemistry Letters, , vol. 11, # 4 p. 541 - 544

~%

2-(2-呋喃基)-4-喹啉羧酸结构式

2-(2-呋喃基)-4-喹啉羧酸

20146-25-2

文献:Gazzetta Chimica Italiana, , vol. 66, p. 452,453 Anm. 5

~%

2-(2-呋喃基)-4-喹啉羧酸结构式

2-(2-呋喃基)-4-喹啉羧酸

20146-25-2

文献:C. r. Acad. Roum., , vol. 6, p. 140,145

 2-(2-呋喃基)-4-喹啉羧酸上下游产品

2-(2-呋喃基)-4-喹啉羧酸上游产品  6

2-(2-呋喃基)-4-喹啉羧酸下游产品  0

 2-(2-呋喃基)-4-喹啉羧酸海关

海关编码 2934999090
中文概述 2934999090. 其他杂环化合物. 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
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 2-(2-呋喃基)-4-喹啉羧酸靶点实验

查看更多实验

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: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.
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
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 2-(2-呋喃基)-4-喹啉羧酸英文别名

2-(2-furyl)-4-quinolinecarboxylic acid
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