Interesting facts
Exploring 6-Methyl-1H-Pyrimidine-2,4-Dione
6-Methyl-1H-pyrimidine-2,4-dione is a fascinating compound that belongs to the pyrimidine family, which is known for its role in various biological systems. Here are some interesting facts about this intriguing compound:
- Structure and Variability: The compound features a unique pyrimidine ring structure that provides it with interesting chemical properties. The methyl group at the 6-position plays a crucial role in affecting its reactivity and interactions with other molecules.
- Biological Importance: Pyrimidines are key components in the formation of nucleotides, which are necessary for nucleic acids (DNA and RNA). Thus, 6-methyl-1H-pyrimidine-2,4-dione can serve as a precursor in the synthesis of biologically significant compounds.
- Chemical Reactions: The presence of carbonyl groups in its structure makes this compound an excellent candidate for various chemical reactions, including nucleophilic addition and cyclization reactions. This versatility opens doors for numerous synthetic applications.
- Pharmaceutical Relevance: Compounds derived from pyrimidine have been explored for their potential pharmaceutical applications. There is ongoing research investigating their use in developing new medications, particularly in the areas of anti-cancer and anti-inflammatory drugs.
- Analytical Techniques: Researchers often use various methods, such as NMR spectroscopy and mass spectrometry, to study and characterize 6-methyl-1H-pyrimidine-2,4-dione. These techniques are pivotal in understanding its molecular structure and behavior.
In conclusion, 6-methyl-1H-pyrimidine-2,4-dione is more than just a chemical compound; it’s a potential gateway into the realm of pharmaceuticals and biological chemistry. Its unique structure, coupled with its applications in synthetic chemistry, make it a subject of significant interest among scientists and chemistry enthusiasts alike.
Synonyms
6-METHYLURACIL
2,4-Dihydroxy-6-methylpyrimidine
6-methylpyrimidine-2,4(1H,3H)-dione
4-Methyluracil
6-Methyl-1H-pyrimidine-2,4-dione
6-Methyl-2,4(1H,3H)-pyrimidinedione
2,4(1H,3H)-Pyrimidinedione, 6-methyl-
Uracil, 6-methyl-
2,4-Pyrimidinediol, 6-methyl-
Pseudothymine (VAN)
NSC 9456
2(1H)-Pyrimidinone, 4-hydroxy-6-methyl-
AWD 23-15
CHEBI:74733
HSDB 5508
EINECS 210-949-4
UNII-5O052W0G6I
DTXSID8052308
4-(6)-Methyluracil
AI3-25472
5O052W0G6I
NSC-9456
METHYLURACIL, 4-
6-METHYLURACIL [MI]
6-METHYLURACIL [HSDB]
DTXCID9030880
AWD-23-15
2(1H)-Pyrimidinone, 4-hydroxy-6-methyl-(8CI)
210-949-4
inchi=1/c5h6n2o2/c1-3-2-4(8)7-5(9)6-3/h2h,1h3,(h2,6,7,8,9
pseudothymine
shvcscwhwmsgte-uhfffaoysa-n
626-48-2
6-methylpyrimidine-2,4-diol
MFCD00006028
6-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
CHEMBL1650614
24PYRIMIDINEDIONE6methyl
Metacyl
Methacyl
6-methyl uracil
WLN: T6MVMVJ F1
SCHEMBL60308
4-Methyl-2.6-dioxypyrimidin
METHYLURACIL [WHO-DD]
6-methylpyrimidine-2,4-dione
SCHEMBL21990343
6-Methyluracil, 97% (HPLC)
NSC9456
HMS1762E01
2,4-dihydroxy-6-methyl-pyrimidine
ALBB-022469
BCP26951
HY-Y1125
STR00504
2,3H)-Pyrimidinedione, 6-methyl-
Tox21_304049
BDBM50106396
STL283926
STL426163
6-methyl-2,4(1H,3H)pyrimidinedione
AKOS000120980
AKOS002303990
pyrimidine, 2,4-dihydroxy-6-methyl-
AC-2536
FM09729
SB57748
NCGC00357256-01
BP-12331
CAS-626-48-2
SY001859
6-Methyl-2,4(1H,3H)-pyrimidinedione #
DB-016105
DB-292227
pyrimidine-2,4(1H,3H)-dione, 6-methyl-
2,4-DI HYDROXYL-6-METHYL PYRIMIDINE
CS-0017143
M0454
NS00035117
EN300-17078
A15712
D70607
2,4-Dihydroxy-6-methylpyrimidine;4-Methyluracil
4-hydroxy-6-methyl-1,2-dihydro-pyrimidin-2-one
AB-323/25048156
AG-670/31546061
Q4161980
Z56871945
F0322-0043
6MU
Solubility of 6-methyl-1H-pyrimidine-2,4-dione
6-methyl-1H-pyrimidine-2,4-dione, a compound known for its diverse applications, exhibits distinct solubility properties that can impact its use in various fields. When discussing the solubility of this compound, several key features come into play:
In summary, it is essential to consider these factors when working with 6-methyl-1H-pyrimidine-2,4-dione. Its solubility characteristics not only dictate its ease of use in chemical reactions but also highlight the importance of selecting the appropriate solvent for optimal results. As noted, "solubility is a gateway to the interaction and functionality of chemical compounds," making it a critical area of study in the realm of chemistry.