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吡咯并[1,2-a]喹喔啉

更新时间:2025-08-25 09:00:39

吡咯并[1,2-a]喹喔啉结构式
吡咯并[1,2-a]喹喔啉结构式
品牌特惠专场
常用名 吡咯并[1,2-a]喹喔啉 英文名 Pyrrolo[1,2-a]quinoxaline
CAS号 234-95-7 分子量 168.19500
密度 1.2g/cm3 沸点 275.6ºC at 760mmHg
分子式 C11H8N2 熔点 N/A
MSDS N/A 闪点 120.5ºC

 吡咯并[1,2-a]喹喔啉名称

中文名 吡咯并[1,2-a]喹喔啉
英文名 Pyrrolo[1,2-a]quinoxaline
英文别名 更多

 吡咯并[1,2-a]喹喔啉物理化学性质

密度 1.2g/cm3
沸点 275.6ºC at 760mmHg
分子式 C11H8N2
分子量 168.19500
闪点 120.5ºC
精确质量 168.06900
PSA 17.30000
LogP 2.48750
InChIKey IEOUSWADWJLLCH-UHFFFAOYSA-N
SMILES c1ccc2c(c1)ncc1cccn12
蒸汽压 0.00504mmHg at 25°C
折射率 1.677
储存条件 室温, 密封, 干燥

 吡咯并[1,2-a]喹喔啉安全信息

海关编码 2933990090

 吡咯并[1,2-a]喹喔啉合成线路

~83%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:Reeves, Jonathan T.; Fandrick, Daniel R.; Tan, Zhulin; Song, Jinhua J.; Lee, Heewon; Yee, Nathan K.; Senanayake, Chris H. Journal of Organic Chemistry, 2010 , vol. 75, # 3 p. 992 - 994

~94%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:Kobayashi; Irisawa; Matoba; Matsumoto; Yoneda; Morikawa; Konishi Bulletin of the Chemical Society of Japan, 2001 , vol. 74, # 6 p. 1109 - 1114

~85%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:Mishra, Amita; Batra, Sanjay European Journal of Organic Chemistry, 2010 , # 25 p. 4832 - 4840

~75%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:Korakas, Demetrios; Kimbaris, Athanasios; Varvounis, George Tetrahedron, 1996 , vol. 52, # 32 p. 10751 - 10760

~31%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:De Fatima Pereira, Maria; Thiery, Valerie Organic Letters, 2012 , vol. 14, # 18 p. 4754 - 4757,4

~%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:Reeves, Jonathan T.; Fandrick, Daniel R.; Tan, Zhulin; Song, Jinhua J.; Lee, Heewon; Yee, Nathan K.; Senanayake, Chris H. Journal of Organic Chemistry, 2010 , vol. 75, # 3 p. 992 - 994

~%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:Kobayashi, Kazuhiro; Matoba, Takeshi; Irisawa, Susumu; Matsumoto, Takashi; Morikawa, Osamu; Konishi, Hisatoshi Chemistry Letters, 1998 , # 6 p. 551 - 552

~%

吡咯并[1,2-a]喹喔啉结构式

吡咯并[1,2-a]喹喔啉

234-95-7

文献:Kobayashi, Kazuhiro; Matoba, Takeshi; Irisawa, Susumu; Matsumoto, Takashi; Morikawa, Osamu; Konishi, Hisatoshi Chemistry Letters, 1998 , # 6 p. 551 - 552

 吡咯并[1,2-a]喹喔啉海关

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%

 吡咯并[1,2-a]喹喔啉靶点实验

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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 吡咯并[1,2-a]喹喔啉英文别名

MFCD00004950
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