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7-氟-3-(肟基)吲哚啉-2-酮

更新时间:2025-08-26 19:19:22

7-氟-3-(肟基)吲哚啉-2-酮结构式
7-氟-3-(肟基)吲哚啉-2-酮结构式
品牌特惠专场
常用名 7-氟-3-(肟基)吲哚啉-2-酮 英文名 7-fluoro-3-(hydroxyamino)indol-2-one
CAS号 143884-84-8 分子量 180.13600
密度 1.62g/cm3 沸点 395.9ºC at 760mmHg
分子式 C8H5FN2O2 熔点 248-250ºC
MSDS N/A 闪点 193.2ºC

 7-氟-3-(肟基)吲哚啉-2-酮名称

中文名 7-氟-3-(肟基)吲哚啉-2-酮
英文名 7-fluoro-3-(hydroxyamino)indol-2-one
英文别名 更多

 7-氟-3-(肟基)吲哚啉-2-酮物理化学性质

密度 1.62g/cm3
沸点 395.9ºC at 760mmHg
熔点 248-250ºC
分子式 C8H5FN2O2
分子量 180.13600
闪点 193.2ºC
精确质量 180.03400
PSA 61.69000
LogP 1.09410
InChIKey OCGNSRRMJCCGCE-UHFFFAOYSA-N
SMILES O=Nc1c(O)[nH]c2c(F)cccc12
蒸汽压 6.56E-08mmHg at 25°C
折射率 1.679

 7-氟-3-(肟基)吲哚啉-2-酮MSDS

 7-氟-3-(肟基)吲哚啉-2-酮安全信息

危害码 (欧洲) Xi: Irritant;
海关编码 2933790090

 7-氟-3-(肟基)吲哚啉-2-酮合成线路

~74%

7-氟-3-(肟基)吲哚啉-2-酮结构式

7-氟-3-(肟基)吲哚啉-2-酮

143884-84-8

文献:ASTRAZENECA AB Patent: US2008/318943 A1, 2008 ; Location in patent: Page/Page column 68 ; US 20080318943 A1

~%

7-氟-3-(肟基)吲哚啉-2-酮结构式

7-氟-3-(肟基)吲哚啉-2-酮

143884-84-8

文献:US2006/247442 A1, ; Page/Page column 6 ;

~64%

7-氟-3-(肟基)吲哚啉-2-酮结构式

7-氟-3-(肟基)吲哚啉-2-酮

143884-84-8

文献:Kearney; Harris; Jackson; Joule Synthesis, 1992 , # 8 p. 769 - 772

~%

7-氟-3-(肟基)吲哚啉-2-酮结构式

7-氟-3-(肟基)吲哚啉-2-酮

143884-84-8

文献:Synthesis, , # 8 p. 769 - 772

~%

7-氟-3-(肟基)吲哚啉-2-酮结构式

7-氟-3-(肟基)吲哚啉-2-酮

143884-84-8

文献:Synthesis, , # 8 p. 769 - 772

 7-氟-3-(肟基)吲哚啉-2-酮上下游产品

7-氟-3-(肟基)吲哚啉-2-酮上游产品  4

7-氟-3-(肟基)吲哚啉-2-酮下游产品  1

 7-氟-3-(肟基)吲哚啉-2-酮海关

海关编码 2933790090
中文概述 2933790090 其他内酰胺. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:9.0% 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 2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0%

 7-氟-3-(肟基)吲哚啉-2-酮靶点实验

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: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
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 7-氟-3-(肟基)吲哚啉-2-酮英文别名

7-Fluoroisatin-3-oxime
7-fluoroisatin oxime
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