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5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇

更新时间:2025-09-02 17:51:52

5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇结构式
5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇结构式
品牌特惠专场
常用名 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇 英文名 5-[(2-PHENYLETHYL)AMINO]-1,3,4-THIADIAZOLE-2-THIOL
CAS号 91129-85-0 分子量 237.34400
密度 1.36g/cm3 沸点 364.3ºC at 760mmHg
分子式 C10H11N3S2 熔点 N/A
MSDS N/A 闪点 174.1ºC

 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇名称

中文名 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇
英文名 5-(2-phenylethylamino)-3H-1,3,4-thiadiazole-2-thione
英文别名 更多

 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇物理化学性质

密度 1.36g/cm3
沸点 364.3ºC at 760mmHg
分子式 C10H11N3S2
分子量 237.34400
闪点 174.1ºC
精确质量 237.03900
PSA 104.85000
LogP 2.55440
InChIKey CCTQEHDMZKCPPK-UHFFFAOYSA-N
SMILES S=c1[nH]nc(NCCc2ccccc2)s1
折射率 1.708

 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇安全信息

海关编码 2934999090

 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇合成线路

~66%

5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇结构式

5-[(2-苯基乙基)氨基]-...

91129-85-0

文献:Sangal; Kumar Journal of the Indian Chemical Society, 1988 , vol. 65, # 11 p. 811 - 812

 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇上下游产品

5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇上游产品  2

5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇下游产品  0

 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇海关

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%

 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇靶点实验

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:qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
来源:NCGC
External Id:tdp43-p2-repeat
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 5-[(2-苯基乙基)氨基]-1,3,4-噻二唑-2-硫醇英文别名

5-[(2-phenylethyl)amino]-1,3,4-thiadiazole-2-thiol
5-phenethylamino-3H-[1,3,4]thiadiazole-2-thione
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