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5-(4-甲氧基-苄基)-噻唑-2-基胺

更新时间:2025-09-10 10:29:30

5-(4-甲氧基-苄基)-噻唑-2-基胺结构式
5-(4-甲氧基-苄基)-噻唑-2-基胺结构式
品牌特惠专场
常用名 5-(4-甲氧基-苄基)-噻唑-2-基胺 英文名 5-(4-METHOXYBENZYL)THIAZOL-2-AMINE
CAS号 299953-06-3 分子量 220.29100
密度 N/A 沸点 N/A
分子式 C11H12N2OS 熔点 N/A
MSDS N/A 闪点 N/A

 5-(4-甲氧基-苄基)-噻唑-2-基胺名称

中文名 5-(4-甲氧基-苄基)-噻唑-2-基胺
英文名 5-[(4-methoxyphenyl)methyl]-1,3-thiazol-2-amine
英文别名 更多

 5-(4-甲氧基-苄基)-噻唑-2-基胺物理化学性质

分子式 C11H12N2OS
分子量 220.29100
精确质量 220.06700
PSA 76.38000
LogP 2.90590
InChIKey MSYFQOUPMXMROC-UHFFFAOYSA-N
SMILES COc1ccc(Cc2cnc(N)s2)cc1
储存条件 2-8°C,干燥,密封

 5-(4-甲氧基-苄基)-噻唑-2-基胺安全信息

危害码 (欧洲) Xi
海关编码 2934100090

 5-(4-甲氧基-苄基)-噻唑-2-基胺合成线路

~76%

5-(4-甲氧基-苄基)-噻唑-2-基胺结构式

5-(4-甲氧基-苄基)-噻唑-2-基胺

299953-06-3

文献:DEVELOPMENT CENTER FOR BIOTECHNOLOGY Patent: US2012/172374 A1, 2012 ; Location in patent: Page/Page column 34-35 ;

~61%

5-(4-甲氧基-苄基)-噻唑-2-基胺结构式

5-(4-甲氧基-苄基)-噻唑-2-基胺

299953-06-3

文献:Saulnier, Mark G.; Dodier, Marco; Frennesson, David B.; Langley, David R.; Vyas, Dolatrai M. Organic Letters, 2009 , vol. 11, # 22 p. 5154 - 5157

~79%

5-(4-甲氧基-苄基)-噻唑-2-基胺结构式

5-(4-甲氧基-苄基)-噻唑-2-基胺

299953-06-3

文献:Obushak; Matiichuk; Vasylyshin; Ostapyuk Russian Journal of Organic Chemistry, 2004 , vol. 40, # 3 p. 383 - 389

~%

5-(4-甲氧基-苄基)-噻唑-2-基胺结构式

5-(4-甲氧基-苄基)-噻唑-2-基胺

299953-06-3

文献:Obushak; Matiichuk; Vasylyshin; Ostapyuk Russian Journal of Organic Chemistry, 2004 , vol. 40, # 3 p. 383 - 389

~%

5-(4-甲氧基-苄基)-噻唑-2-基胺结构式

5-(4-甲氧基-苄基)-噻唑-2-基胺

299953-06-3

文献:DEVELOPMENT CENTER FOR BIOTECHNOLOGY Patent: US2012/172374 A1, 2012 ;

~%

5-(4-甲氧基-苄基)-噻唑-2-基胺结构式

5-(4-甲氧基-苄基)-噻唑-2-基胺

299953-06-3

文献:DEVELOPMENT CENTER FOR BIOTECHNOLOGY Patent: US2012/172374 A1, 2012 ;

 5-(4-甲氧基-苄基)-噻唑-2-基胺上下游产品

5-(4-甲氧基-苄基)-噻唑-2-基胺上游产品  6

5-(4-甲氧基-苄基)-噻唑-2-基胺下游产品  0

 5-(4-甲氧基-苄基)-噻唑-2-基胺海关

海关编码 2934100090
中文概述 2934100090. 结构上含有一个非稠合噻唑环的化合物(不论是否氢化). 增值税率:17.0%. 退税率:9.0%. 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 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 5-(4-甲氧基-苄基)-噻唑-2-基胺靶点实验

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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: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
实验名称:qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
来源:NCGC
External Id:tdp43-p2-repeat
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 5-(4-甲氧基-苄基)-噻唑-2-基胺英文别名

MFCD00706169
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