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(5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐

更新时间:2025-09-18 16:46:12

(5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐结构式
(5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐结构式
品牌特惠专场
常用名 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐 英文名 (5-Amino-2H-1,2,4-Triazol-3-Yl)Methanol
CAS号 63870-39-3 分子量 114.106
密度 1.6±0.1 g/cm3 沸点 461.3±47.0 °C at 760 mmHg
分子式 C3H6N4O 熔点 N/A
MSDS N/A 闪点 232.8±29.3 °C

 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐名称

中文名 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇
英文名 (5-amino-1h-1,2,4-triazol-3-yl)methanol
英文别名 更多

 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐物理化学性质

密度 1.6±0.1 g/cm3
沸点 461.3±47.0 °C at 760 mmHg
分子式 C3H6N4O
分子量 114.106
闪点 232.8±29.3 °C
精确质量 114.054161
PSA 87.82000
LogP -1.79
InChIKey XUGNFVGSBRYXGB-UHFFFAOYSA-N
SMILES Nc1n[nH]c(CO)n1.O=C(O)CO
蒸汽压 0.0±1.2 mmHg at 25°C
折射率 1.713
储存条件 2-8°C

 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐安全信息

危害码 (欧洲) Xi
海关编码 2933990090

 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐合成线路

~82%

(5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐结构式

(5-氨基-1H-1,2,4-...

63870-39-3

文献:COCRYSTAL DISCOVERY, INC.; LEE, Sam, Sk; SHEN, Wang; ZHENG, Xiaoliang; JACOBSON, Irina, C. Patent: WO2012/83105 A1, 2012 ; Location in patent: Page/Page column 101 ; WO 2012/083105 A1

 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐上下游产品

(5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐上游产品  2

(5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐下游产品  2

 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐海关

海关编码 2933990090
中文概述 2933990090. 其他仅含氮杂原子的杂环化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 (5-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐靶点实验

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: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: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: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: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-氨基-1H-1,2,4-噻唑-3-基)甲醇乙醇酸盐英文别名

(3-Amino-1H-1,2,4-triazol-5-yl)methanol
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