M6631
3-Methyluracil
Sinónimos:
3-MeU
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About This Item
Fórmula empírica (notación de Hill):
C5H6N2O2
Número de CAS:
Peso molecular:
126.11
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.51
Productos recomendados
assay
≥98% (TLC)
Quality Level
form
powder
solubility
1 M NaOH: 50 mg/mL, clear, colorless to faintly yellow
storage temp.
−20°C
SMILES string
CN1C(=O)NC=CC1=O
InChI
1S/C5H6N2O2/c1-7-4(8)2-3-6-5(7)9/h2-3H,1H3,(H,6,9)
InChI key
VPLZGVOSFFCKFC-UHFFFAOYSA-N
General description
3-Methyluracil is a methylated uracil or a uracil derivative.
Application
3-Methyluracil (3-MeU) is used along with other methyl-pyrimidines to study relative physical chemical parameters.
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T V Chestnova et al.
Bulletin of experimental biology and medicine, 165(6), 777-780 (2018-10-26)
Bacterial biofilms provoke and/or promote the most chronic and recurrent infectious diseases. Previously, experimental models of purulent peritonitis and meningoencephalitis revealed positive antibiofilm effect of metallic nanoparticles and the absence of resistance against such nanoparticles in microorganisms. This study examines
Vibrational Feshbach resonances in uracil and thymine.
Burrow PD, Gallup GA, et al.
J. Chem. Phys. , 28, 124310-124310 (2006)
A Nyéki et al.
British journal of clinical pharmacology, 55(1), 62-67 (2003-01-22)
(i) To compare the phenotyping of healthy subjects for NAT2 and CYP1A2 activities with caffeine, by the simultaneous assay of the urinary metabolites AFMU and AAMU, and (ii) to ascertain whether NAT2 and CYP1A2 phenotyping is influenced by the use
Mihajlo Etinski et al.
Physical chemistry chemical physics : PCCP, 12(19), 4915-4923 (2010-05-07)
In this work we investigated the lowest-lying electronic excitations for a series of methyl-substituted uracil derivatives, i.e., uracil, 1-methyluracil, 3-methyluracil, thymine, 1-methylthymine, 1,3-dimethyluracil, 3-methylthymine, 1,3-dimethylthymine, and their microhydrated complexes by means of coupled cluster singles and approximate doubles (CC2) and
P D Burrow et al.
The Journal of chemical physics, 124(12), 124310-124310 (2006-04-08)
Sharp peaks in the dissociative electron attachment (DEA) cross sections of uracil and thymine at energies below 3 eV are assigned to vibrational Feshbach resonances (VFRs) arising from coupling between the dipole bound state and the temporary anion state associated
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