120618
4-Hydroxypyridine
95%
Synonym(s):
4-Pyridinol, 4-Pyridone
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About This Item
Empirical Formula (Hill Notation):
C5H5NO
CAS Number:
Molecular Weight:
95.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-958-3
Beilstein/REAXYS Number:
105800
MDL number:
Assay:
95%
InChI key
GCNTZFIIOFTKIY-UHFFFAOYSA-N
InChI
1S/C5H5NO/c7-5-1-3-6-4-2-5/h1-4H,(H,6,7)
SMILES string
O=C1C=CNC=C1
assay
95%
bp
230-235 °C/12 mmHg (lit.)
mp
150-151 °C (lit.)
Quality Level
Application
4-Hydroxypyridine was used in the synthesis of (Ag3MoO3F3) (Ag3MoO4)Cl by hydro(solvato)thermal methods. It was used as model compound to study the natural photodegradation of representative aquatic environmental contaminants.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Heiko Zettl et al.
ACS chemical biology, 7(9), 1488-1495 (2012-06-26)
We present an integrated approach to identify and optimize a novel class of γ-secretase modulators (GSMs) with a unique pharmacological profile. Our strategy included (i) virtual screening through application of a recently developed protocol (PhAST), (ii) synthetic chemistry to discover
Modelling the natural photodegradation of water contaminants: a kinetic study on the light-induced aerobic interactions between riboflavin and 4-hydroxypyridine.
Pajares A, et al.
J. Photochem. Photobiol., A, 139(2), 199-204 (2001)
H Chen et al.
Biochemistry, 32(43), 11591-11599 (1993-11-02)
We have examined the interaction of Citrobacter freundii tyrosine phenol-lyase with both L- and D-alanine. This enzyme catalyzes the racemization of alanine as a side reaction, in addition to the physiological beta-elimination of L-tyrosine to give phenol and ammonium pyruvate.
Alignment of acentric MoO3F33-anions in a polar material :(AgMoO3F3)(Ag3MoO4) Cl.
Maggard PA, et al.
Journal of Solid State Chemistry, 175(1), 27-33 (2003)
Natsuki K Kubota et al.
Bioorganic & medicinal chemistry, 11(21), 4569-4575 (2003-10-07)
Piericidins C5 (1) and C6 (2), two new members of the piericidin family, were isolated from a Streptomyces sp. and a Nocardioides sp., together with known piericidins C1 (3), C2 (4), C3 (5), C4 (6), D1 (7), and A3 (8).
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