H57009
3-羟基吡啶
98%
别名:
3-吡啶酚, 3-吡啶酮
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关于此项目
经验公式（希尔记法）:
C5H5NO
化学文摘社编号:
分子量:
95.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-637-4
Beilstein/REAXYS Number:
105699
MDL number:
Assay:
98%
InChI key
GRFNBEZIAWKNCO-UHFFFAOYSA-N
InChI
1S/C5H5NO/c7-5-2-1-3-6-4-5/h1-4,7H
SMILES string
Oc1cccnc1
assay
98%
Quality Level
mp
125-128 °C (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Misaki Nakai et al.
Journal of inorganic biochemistry, 99(6), 1275-1282 (2005-05-27)
Metal complexes of 3-hydroxypyridine-2-carboxylic acid (H(2)hpic), [Co(Hhpic)(2)(H(2)O)(2)] (1), [Fe(Hhpic)(2)(H(2)O)(2)] (2), [Zn(Hhpic)(2)(H(2)O)(2)] (3), [Mn(Hhpic)(2)(H(2)O)(2)] (4), and [Cu(Hhpic)(2)] (5) have been synthesized and characterized by mass spectrometry, elemental analysis, magnetic susceptibility, infrared, electronic absorption and electron paramagnetic resonance (EPR) spectroscopies. The solid-state
Hye-Young Kim et al.
Journal of medicinal chemistry, 48(22), 6787-6789 (2005-10-28)
Because alpha-tocopherol (alpha-TOH) mediates the peroxidation of cholesterol-esterified lipids in human low-density lipoprotein (LDL) in vitro and has displayed disappointing results against the onset and development of atherosclerosis, it may not be appropriate for use as a therapeutic in the
Stefica Horvat et al.
Chemical biology & drug design, 70(1), 30-39 (2007-07-17)
The kinetics of formation and identity of the reaction products of the glucuronic acid with three representative opioid peptides were investigated in vitro. Peptides were conjugated with glucuronic acid either in solution or under dry-heating conditions. From the incubations performed
Molecular modeling analysis: "Why is 2-hydroxypyridine soluble in water but not 3-hydroxypyridine?".
Fazlul Huq et al.
Journal of molecular modeling, 8(3), 81-86 (2002-07-12)
Molecular mechanics and semiempirical calculations using HyperChem 5 were carried out to investigate whether the results obtained can explain why 2-hydroxypyridine is far more soluble in water than 3-hydroxypyridine. The results of molecular mechanics calculations show that in solution in
E B Watkins et al.
Bioorganic & medicinal chemistry letters, 11(16), 2099-2100 (2001-08-22)
Tyrosine phenol-lyase from Citrobacter freundii synthesizes 2-aza-L-tyrosine and 3-aza-L-tyrosine from 3-hydroxypyridine and 2-hydroxypyridine, respectively, and ammonium pyruvate.
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