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3,5-二碘吡啶-2-醇

更新时间:2025-08-26 17:02:17

3,5-二碘吡啶-2-醇结构式
3,5-二碘吡啶-2-醇结构式
品牌特惠专场
常用名 3,5-二碘吡啶-2-醇 英文名 3,5-diiodo-2-pyridinol
CAS号 13472-80-5 分子量 346.892
密度 2.8±0.1 g/cm3 沸点 375.8±42.0 °C at 760 mmHg
分子式 C5H3I2NO 熔点 N/A
MSDS N/A 闪点 181.1±27.9 °C

 3,5-二碘吡啶-2-醇名称

中文名 3,5-二碘吡啶-2-醇
英文名 3,5-diiodo-1H-pyridin-2-one
英文别名 更多

 3,5-二碘吡啶-2-醇物理化学性质

密度 2.8±0.1 g/cm3
沸点 375.8±42.0 °C at 760 mmHg
分子式 C5H3I2NO
分子量 346.892
闪点 181.1±27.9 °C
精确质量 346.830383
PSA 32.86000
LogP 1.58
InChIKey JYLBTESOPCUQIT-UHFFFAOYSA-N
SMILES O=c1[nH]cc(I)cc1I
蒸汽压 0.0±0.9 mmHg at 25°C
折射率 1.770
储存条件 室温,避光,保存于惰性气体中

 3,5-二碘吡啶-2-醇合成线路

~78%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

文献:Rousseau, Gerard; Robin, Sylvie Tetrahedron Letters, 1997 , vol. 38, # 14 p. 2467 - 2470

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

文献:Rodewald Roczniki Chemii, 1938 , vol. 18, p. 96,100 Chem. Zentralbl., 1939 , vol. 110, # II p. 643

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

文献:Rodewald Roczniki Chemii, 1938 , vol. 18, p. 96,100 Chem. Zentralbl., 1939 , vol. 110, # II p. 643

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

文献:Pfeiffer Chemische Berichte, 1887 , vol. 20, p. 1351

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

文献:Sugii; Shindo Yakugaku Zasshi, 1931 , vol. 51, p. 416 Chem.Abstr., 1931 , p. 4549

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

文献:Rodewald Roczniki Chemii, 1938 , vol. 18, p. 96,100 Chem. Zentralbl., 1939 , vol. 110, # II p. 643

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

文献:Rodewald Roczniki Chemii, 1938 , vol. 18, p. 96,100 Chem. Zentralbl., 1939 , vol. 110, # II p. 643

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

详细
文献:Rodewald Roczniki Chemii, 1938 , vol. 18, p. 96,100 Chem. Zentralbl., 1939 , vol. 110, # II p. 643

~%

3,5-二碘吡啶-2-醇结构式

3,5-二碘吡啶-2-醇

13472-80-5

详细
文献:Rodewald Roczniki Chemii, 1938 , vol. 18, p. 96,100 Chem. Zentralbl., 1939 , vol. 110, # II p. 643

 3,5-二碘吡啶-2-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: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
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 3,5-二碘吡啶-2-醇英文别名

T6MVJ CI EI
3,5-Diiodo-2-pyridol
3,5-diiodo-2-pyridinol
3,5-Dijod-pyridin-2-ol
3,5-diiodopyridin-2-ol
2-Hydroxy-3,5-dijod-pyridin
2-hydroxy-3,5-diiodopyridine
3,5-Diiodopyridin-2(1H)-one
T6NJ BQ CI EI
2-Hydroxy-3,5-diiod-pyridin
3,5-diiodo-2(1H)-pyridone
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