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1-(4-氟苄基)-1H-吲哚-3-甲醛

更新时间:2025-09-21 19:13:26

1-(4-氟苄基)-1H-吲哚-3-甲醛结构式
1-(4-氟苄基)-1H-吲哚-3-甲醛结构式
品牌特惠专场
常用名 1-(4-氟苄基)-1H-吲哚-3-甲醛 英文名 1-(4-FLUORO-BENZYL)-1H-INDOLE-3-CARBALDEHYDE
CAS号 192997-23-2 分子量 253.27100
密度 1.17g/cm3 沸点 443.9ºC at 760 mmHg
分子式 C16H12FNO 熔点 N/A
MSDS N/A 闪点 222.3ºC

 1-(4-氟苄基)-1H-吲哚-3-甲醛名称

中文名 1-(4-氟苄基)-1H-吲哚-3-甲醛
英文名 1-[(4-fluorophenyl)methyl]indole-3-carbaldehyde

 1-(4-氟苄基)-1H-吲哚-3-甲醛物理化学性质

密度 1.17g/cm3
沸点 443.9ºC at 760 mmHg
分子式 C16H12FNO
分子量 253.27100
闪点 222.3ºC
精确质量 253.09000
PSA 22.00000
LogP 3.64120
InChIKey NZBLQHFUUZBVFC-UHFFFAOYSA-N
SMILES O=Cc1cn(Cc2ccc(F)cc2)c2ccccc12
蒸汽压 4.45E-08mmHg at 25°C
折射率 1.595

 1-(4-氟苄基)-1H-吲哚-3-甲醛安全信息

危害码 (欧洲) Xi: Irritant;
海关编码 2933990090

 1-(4-氟苄基)-1H-吲哚-3-甲醛合成线路

~73%

1-(4-氟苄基)-1H-吲哚-3-甲醛结构式

1-(4-氟苄基)-1H-吲哚-3-甲醛

192997-23-2

文献:Wang, Guangcheng; Li, Chunyan; He, Lin; Lei, Kai; Wang, Fang; Pu, Yuzi; Yang, Zhuang; Cao, Dong; Ma, Liang; Chen, Jinying; Sang, Yun; Liang, Xiaolin; Xiang, Mingli; Peng, Aihua; Wei, Yuquan; Chen, Lijuan Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 7 p. 2060 - 2079

~77%

1-(4-氟苄基)-1H-吲哚-3-甲醛结构式

1-(4-氟苄基)-1H-吲哚-3-甲醛

192997-23-2

文献:Battaglia, Sandra; Boldrini, Enrico; Da Settimo, Federico; Dondio, Giulio; La Motta, Concettina; Marini, Anna Maria; Primofiore, Giampaolo European Journal of Medicinal Chemistry, 1999 , vol. 34, # 2 p. 93 - 105

~%

1-(4-氟苄基)-1H-吲哚-3-甲醛结构式

1-(4-氟苄基)-1H-吲哚-3-甲醛

192997-23-2

文献:Reddy, Y. Thirupathi; Sekhar, Konjeti R.; Sasi, Nidhish; Reddy, P. Narsimha; Freeman, Michael L.; Crooks, Peter A. Bioorganic and Medicinal Chemistry Letters, 2010 , vol. 20, # 2 p. 600 - 602

~%

1-(4-氟苄基)-1H-吲哚-3-甲醛结构式

1-(4-氟苄基)-1H-吲哚-3-甲醛

192997-23-2

文献:Na, Young Min Bulletin of the Korean Chemical Society, 2011 , vol. 32, # 1 p. 307 - 310

 1-(4-氟苄基)-1H-吲哚-3-甲醛上下游产品

1-(4-氟苄基)-1H-吲哚-3-甲醛上游产品  4

1-(4-氟苄基)-1H-吲哚-3-甲醛下游产品  0

 1-(4-氟苄基)-1H-吲哚-3-甲醛海关

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%

 1-(4-氟苄基)-1H-吲哚-3-甲醛靶点实验

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: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:Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for Validation...
来源:NMMLSC
靶标:ATP-binding cassette sub-family B member 6, mitochondrial [Homo sapiens]
External Id:UNMCMD_ABCB6_1o_ValidationSet
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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