122505
2,3-二羟基吡啶
95%
别名:
2,3-吡啶二醇
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关于此项目
经验公式（希尔记法）:
C5H5NO2
化学文摘社编号:
分子量:
111.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
240-887-3
Beilstein/REAXYS Number:
109848
MDL number:
产品名称
2,3-二羟基吡啶, 95%
InChI key
GGOZGYRTNQBSSA-UHFFFAOYSA-N
InChI
1S/C5H5NO2/c7-4-2-1-3-6-5(4)8/h1-3,7H,(H,6,8)
SMILES string
Oc1cccnc1O
assay
95%
mp
245 °C (dec.) (lit.)
Quality Level
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Application
2,3-二羟基吡啶（DHP）用于通过偶氮偶合剂合成DHP负载的Amberlite XAD-2。 通过使用连接基团 -NH-CH2-CH2-NH-SO2-C6H4-N=N- 和 -SO2-C6H4-N=N将DHP负载在纤维素上，可将DHP用于合成新型大分子螯合剂。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Lei Wang et al.
European journal of medicinal chemistry, 156, 680-691 (2018-07-23)
Human immunodeficiency virus (HIV) reverse transcriptase (RT)-associated ribonuclease H (RNase H) remains an unvalidated drug target. Reported HIV RNase H inhibitors generally lack significant antiviral activity. We report herein the design, synthesis, biochemical and antiviral evaluations of a new 6-biphenylmethyl
Jayakanth Kankanala et al.
European journal of medicinal chemistry, 141, 149-161 (2017-10-17)
Human immunodeficiency virus (HIV) reverse transcriptase (RT) associated ribonuclease H (RNase H) is the only HIV enzymatic function not targeted by current antiviral drugs. Although various chemotypes have been reported to inhibit HIV RNase H, few have shown significant antiviral
James M Harrington et al.
Inorganic chemistry, 49(18), 8208-8221 (2010-08-19)
The synthesis of a novel class of exocyclic bis- and tris-3,2-hydroxypyridinone (HOPO) chelators built on N(2) and N(3) aza-macrocyclic scaffolds and the thermodynamic solution characterization of their complexes with Fe(III) are described. The chelators for this study were prepared by
Ruminal motility in sheep intoxicated with 2,3-dihydroxypyridine.
C S McSweeney et al.
Australian veterinary journal, 61(8), 271-272 (1984-08-01)
Vibha Gurnani et al.
Analytical and bioanalytical chemistry, 377(6), 1079-1086 (2003-08-09)
New macromolecular chelators have been synthesized, by loading 2,3-dihydroxypyridine (DHP) on cellulose via linkers -NH-CH(2)-CH(2)-NH-SO(2)-C(6)H(4)-N=N- and -SO(2)-C(6)H(4)-N=N-, and characterized by elemental analysis, TGA, IR, and CPMAS (13)C NMR spectra. The cellulose with DHP anchored by the shorter linker had better
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