Merck
CN

122505

Sigma-Aldrich

2,3-二羟基吡啶

95%

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别名:
2,3-吡啶二醇
经验公式(希尔记法):
C5H5NO2
CAS号:
分子量:
111.10
Beilstein:
109848
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

检测方案

95%

mp

245 °C (dec.) (lit.)

SMILES string

Oc1cccnc1O

InChI

1S/C5H5NO2/c7-4-2-1-3-6-5(4)8/h1-3,7H,(H,6,8)

InChI key

GGOZGYRTNQBSSA-UHFFFAOYSA-N

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应用

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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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
R J Jones et al.
Australian veterinary journal, 63(8), 259-262 (1986-08-01)
Cattle and goats in Australia lack the ability to totally degrade 3-hydroxy-4(1H)-pyridone, also known as 3,4-dihydroxy pyridine (3,4 DHP), the ruminal metabolite of mimosine, a toxic aminoacid present in the leguminous shrub Leucaena leucocephala. Ruminants in Hawaii have this capacity
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)

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