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5-异丁基-[1,3,4]噻唑-2-胺

更新时间:2025-08-25 18:44:01

5-异丁基-[1,3,4]噻唑-2-胺结构式
5-异丁基-[1,3,4]噻唑-2-胺结构式
品牌特惠专场
常用名 5-异丁基-[1,3,4]噻唑-2-胺 英文名 5-(2-methylpropyl)-1,3,4-thiadiazol-2-amine
CAS号 52057-89-3 分子量 157.23700
密度 1.174g/cm3 沸点 280.8ºC at 760 mmHg
分子式 C6H11N3S 熔点 N/A
MSDS N/A 闪点 123.6ºC

 5-异丁基-[1,3,4]噻唑-2-胺名称

中文名 5-异丁基-[1,3,4]噻唑-2-胺
英文名 5-(2-methylpropyl)-1,3,4-thiadiazol-2-amine
中文别名 5-异丁基-[1,3,4]噻二唑-2-胺
英文别名 更多

 5-异丁基-[1,3,4]噻唑-2-胺物理化学性质

密度 1.174g/cm3
沸点 280.8ºC at 760 mmHg
分子式 C6H11N3S
分子量 157.23700
闪点 123.6ºC
精确质量 157.06700
PSA 80.04000
LogP 1.90000
InChIKey GOGZJIYMDRZJII-UHFFFAOYSA-N
SMILES CC(C)Cc1nnc(N)s1
折射率 1.568

 5-异丁基-[1,3,4]噻唑-2-胺安全信息

海关编码 2934999090

 5-异丁基-[1,3,4]噻唑-2-胺上下游产品

5-异丁基-[1,3,4]噻唑-2-胺上游产品  4

5-异丁基-[1,3,4]噻唑-2-胺下游产品  1

 5-异丁基-[1,3,4]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%

 5-异丁基-[1,3,4]噻唑-2-胺靶点实验

查看更多实验

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:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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: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:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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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 5-异丁基-[1,3,4]噻唑-2-胺英文别名

2-amino-5-isobutyl-1,3,4-thiadiazole
2-Amino-5-isobutyl-1,3,4-thiadiazol
5-isobutyl-1,3,4-thiadiazol-2-amine
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