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3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole

更新时间:2025-09-18 18:45:51

3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole结构式
3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole结构式
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常用名 3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole 英文名 3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole
CAS号 7496-59-5 分子量 281.17200
密度 1.68g/cm3 沸点 396.4ºC at 760mmHg
分子式 C11H9BrN2S 熔点 N/A
MSDS N/A 闪点 193.5ºC

 名称

英文名 3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole
英文别名 更多

 物理化学性质

密度 1.68g/cm3
沸点 396.4ºC at 760mmHg
分子式 C11H9BrN2S
分子量 281.17200
闪点 193.5ºC
精确质量 279.96700
PSA 45.53000
LogP 2.32900
InChIKey PVPFCMJKVBCGES-UHFFFAOYSA-N
SMILES Brc1ccc(C2=CSC3=NCCN23)cc1

 合成线路

~46%

3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole结构式

3-(4-bromopheny...

7496-59-5

文献:Mohan; Verma; Singh Synthetic Communications, 1992 , vol. 22, # 9 p. 1293 - 1298

~%

3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole结构式

3-(4-bromopheny...

7496-59-5

文献:Fefer,M.; King,L.C. Journal of Organic Chemistry, 1961 , vol. 26, p. 828 - 835

~%

3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole结构式

3-(4-bromopheny...

7496-59-5

文献:Sharpe,C.J. et al. Journal of Medicinal Chemistry, 1971 , vol. 14, # 10 p. 977 - 982

~%

3-(4-bromophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole结构式

3-(4-bromopheny...

7496-59-5

文献:Prakash, Om; Rani, Neena; Goyal, Seema Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1992 , # 6 p. 707 - 710

 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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 英文别名

3-(4-bromo-phenyl)-5,6-dihydro-imidazo[2,1-b]thiazole
3-p-bromophenyl-5,6-dihydro-4H-imidazo<2,1-b>thiazole
3-(p-Bromphenyl)-5,6-dihydro-imidazo<2,1-b>thiazol
3-(4-bromophenyl)-5-(4-methoxyphenyl)[1,2,4]oxadiazole
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