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4-(2-呋喃)-1,3-噻唑-2-胺

更新时间:2025-08-28 20:20:11

4-(2-呋喃)-1,3-噻唑-2-胺结构式
4-(2-呋喃)-1,3-噻唑-2-胺结构式
品牌特惠专场
常用名 4-(2-呋喃)-1,3-噻唑-2-胺 英文名 2-Thiazol amine,4-(2-furanyl)
CAS号 28989-52-8 分子量 166.200
密度 1.4±0.1 g/cm3 沸点 337.9±17.0 °C at 760 mmHg
分子式 C7H6N2OS 熔点 N/A
MSDS N/A 闪点 158.1±20.9 °C

 4-(2-呋喃)-1,3-噻唑-2-胺名称

中文名 4-(2-呋喃)-1,3-噻唑-2-胺
英文名 4-(furan-2-yl)-1,3-thiazol-2-amine
中文别名 4-(呋喃-2-基)噻唑-2-胺 | 2-噻唑胺,4-(2-呋喃基)
英文别名 更多

 4-(2-呋喃)-1,3-噻唑-2-胺物理化学性质

密度 1.4±0.1 g/cm3
沸点 337.9±17.0 °C at 760 mmHg
分子式 C7H6N2OS
分子量 166.200
闪点 158.1±20.9 °C
精确质量 166.020081
PSA 80.29000
LogP 1.33
InChIKey CGJGALUSBPYALD-UHFFFAOYSA-N
SMILES Nc1nc(-c2ccco2)cs1
蒸汽压 0.0±0.7 mmHg at 25°C
折射率 1.635

 4-(2-呋喃)-1,3-噻唑-2-胺MSDS

 4-(2-呋喃)-1,3-噻唑-2-胺安全信息

海关编码 2934100090

 4-(2-呋喃)-1,3-噻唑-2-胺合成线路

~%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:Genelabs Technologies, Inc. Patent: US2007/265265 A1, 2007 ; Location in patent: Page/Page column 102 ;

~%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:KYOWA HAKKO KOGYO CO., LTD. Patent: EP1894930 A1, 2008 ; Location in patent: Page/Page column 33-34 ; EP 1894930 A1

~%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:Zhu, Yan-Ping; Yuan, Jing-Jing; Zhao, Qin; Lian, Mi; Gao, Qing-He; Liu, Mei-Cai; Yang, Yan; Wu, An-Xin Tetrahedron, 2012 , vol. 68, # 1 p. 173 - 178

~72%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:Ueno, Makoto; Togo, Hideo Synthesis, 2004 , # 16 p. 2673 - 2677

~65%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:Singh, Shiv P.; Naithani, Rajesh; Aggarwal, Ranjana; Prakash, Om Synthetic Communications, 1998 , vol. 28, # 13 p. 2371 - 2378

~%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:Singh, Shiv P.; Naithani, Rajesh; Aggarwal, Ranjana; Prakash, Om Synthetic Communications, 1998 , vol. 28, # 13 p. 2371 - 2378

~%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:Knott Journal of the Chemical Society, 1947 , p. 1656,1658

~%

4-(2-呋喃)-1,3-噻唑-2-胺结构式

4-(2-呋喃)-1,3-噻唑-2-胺

28989-52-8

文献:Knott Journal of the Chemical Society, 1947 , p. 1656,1658

 4-(2-呋喃)-1,3-噻唑-2-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%

 4-(2-呋喃)-1,3-噻唑-2-胺靶点实验

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: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
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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 4-(2-呋喃)-1,3-噻唑-2-胺英文别名

F0863-0373
4-furan-2-yl-thiazol-2-ylamine
4-(2-Furyl)-1,3-thiazol-2-amine
2-Thiazol amine,4-(2-furanyl)
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