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4-(吗啉甲基)噻唑-2-胺

更新时间:2025-08-20 18:33:36

4-(吗啉甲基)噻唑-2-胺结构式
4-(吗啉甲基)噻唑-2-胺结构式
品牌特惠专场
常用名 4-(吗啉甲基)噻唑-2-胺 英文名 2-Thiazolamine,4-(4-morpholinylmethyl)
CAS号 3008-61-5 分子量 200.281
密度 1.312g/cm3 沸点 346.5±27.0 °C at 760 mmHg
分子式 C8H14N3OS 熔点 N/A
MSDS N/A 闪点 163.3±23.7 °C

 4-(吗啉甲基)噻唑-2-胺名称

中文名 4-(吗啉-4-甲基)-1,3-噻唑-2-胺
英文名 4-(morpholin-4-ylmethyl)-1,3-thiazol-2-amine
中文别名 4-(4-吗啉基甲基)噻唑-2-胺
英文别名 更多

 4-(吗啉甲基)噻唑-2-胺物理化学性质

密度 1.312g/cm3
沸点 346.5±27.0 °C at 760 mmHg
分子式 C8H14N3OS
分子量 200.281
闪点 163.3±23.7 °C
精确质量 200.085205
PSA 79.62000
LogP -0.66
InChIKey GSAMTLRIAXVZHZ-UHFFFAOYSA-N
SMILES Nc1nc(CN2CCOCC2)cs1
外观性状 浅黄色至黄色固体
蒸汽压 0.0±0.8 mmHg at 25°C
折射率 1.622
储存条件 2-8°C, 避光

 4-(吗啉甲基)噻唑-2-胺MSDS

 4-(吗啉甲基)噻唑-2-胺安全信息

危害码 (欧洲) Xn
海关编码 2934999090

 4-(吗啉甲基)噻唑-2-胺合成线路

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4-(吗啉甲基)噻唑-2-胺结构式

4-(吗啉甲基)噻唑-2-胺

3008-61-5

文献:SIRTRIS PHARMACEUTICALS, INC.; VU, Chi, B. Patent: WO2010/19606 A1, 2010 ; Location in patent: Page/Page column 80-81 ; WO 2010/019606 A1

~%

4-(吗啉甲基)噻唑-2-胺结构式

4-(吗啉甲基)噻唑-2-胺

3008-61-5

文献:BOEHRINGER INGELHEIM INTERNATIONAL GMBH; BOEHRINGER INGELHEIM PHARMA GMBH and CO. KG Patent: WO2008/86047 A1, 2008 ; Location in patent: Page/Page column 153-154 ; WO 2008/086047 A1

 4-(吗啉甲基)噻唑-2-胺上下游产品

4-(吗啉甲基)噻唑-2-胺上游产品  2

4-(吗啉甲基)噻唑-2-胺下游产品  0

 4-(吗啉甲基)噻唑-2-胺海关

海关编码 2934999090
中文概述 2934999090. 其他杂环化合物. 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
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 4-(吗啉甲基)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:Confirmed allosteric antagonists of M1 Muscarinic receptor
来源:1043
靶标:Muscarinic acetylcholine receptor M1
External Id:SAID_435034
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: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-(吗啉甲基)噻唑-2-胺英文别名

F2158-0442
4-(morpholinomethyl)thiazol-2-amine
4-[(2-Amino-1,3-thiazol-4-yl)methyl]morpholin-4-ium
4-Morpholin-4-ylmethyl-thiazol-2-ylamine
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