Interesting facts
Interesting Facts about 5-Chloro-1H-pyrimidine-2,4-dione
5-Chloro-1H-pyrimidine-2,4-dione is a fascinating compound that occupies a notable space in the field of organic chemistry. This compound belongs to the pyrimidine family, which is characterized by a six-membered ring containing two nitrogen atoms at positions 1 and 3. Here are some engaging insights into this intriguing compound:
- Key Structural Features: The presence of the chlorine atom at the 5-position enhances the reactivity of the molecule, making it a versatile intermediate in various chemical reactions.
- Biological Relevance: Compounds related to pyrimidine derivatives have been widely studied for their biological activities, especially in the development of pharmaceuticals. This particular compound may have potential applications in medicinal chemistry.
- Synthesis Pathways: 5-Chloro-1H-pyrimidine-2,4-dione can be synthesized through several methods, including the reaction of barbituric acid with reagents like thionyl chloride. These methods are crucial for producing derivatives that can be used in various applications.
- Research Potential: Given its structure, there is ongoing research into the compound’s reactivity and potential applications in synthetic chemistry, including its use as a building block for more complex molecules.
- Applications in Material Science: The compound's unique chemical properties can lend themselves to applications in material science, particularly in developing novel materials with specific functionalities.
Overall, 5-chloro-1H-pyrimidine-2,4-dione is not just a simple molecule; its unique structure and chemical properties open doors to various research avenues and potential applications across different scientific fields.
Synonyms
5-CHLOROURACIL
1820-81-1
2,4(1H,3H)-Pyrimidinedione, 5-chloro-
5-chloropyrimidine-2,4(1H,3H)-dione
5-Chloro-2,4-dihydroxypyrimidine
Uracil, 5-chloro-
CHEBI:60762
EINECS 217-339-7
7LQ4V03RNY
NSC 28172
AI3-26560
NSC-28172
CHLOROURACIL, 5-
5-chloro-2,4-pyrimidinedione
DTXSID7075137
FLUOROURACIL IMPURITY E [EP IMPURITY]
FLUOROURACIL IMPURITY E (EP IMPURITY)
Uracil, 5-chloro-(VAN)
DTXCID6035788
Uracil, 5-chloro-(VAN) (8CI)
217-339-7
inchi=1/c4h3cln2o2/c5-2-1-6-4(9)7-3(2)8/h1h,(h2,6,7,8,9
5-Chloro-1H-pyrimidine-2,4-dione
5-chloro-uracil
MFCD00006019
164415-64-9
4(3H)-Pyrimidinone, 5-chloro-2-hydroxy- (9CI)
2,4-Pyrimidinediol, 5-chloro- (9CI)
NSC28172
107577-08-2
210369-56-5
5-Chlorouracil (Fluorouracil Impurity)
UNII-7LQ4V03RNY
Uracil, 5-chloro- (VAN)
Fluorouracil Impurity E
Epitope ID:138111
SCHEMBL42227
CHEMBL144082
5-Chloropyrimidine-2,4(1H,3H)-dione (5-Chlorouracil)
HY-I0959
2,3H)-Pyrimidinedione, 5-chloro-
AKOS003093906
AKOS003242135
AKOS006222774
AC-8694
FC05961
SB57723
5-Chlorouracil, ReagentPlus(R), 99%
AS-10925
NCI60_002298
PD121670
SY028182
5-Chloro-2,4(1H,3H)-pyrimidinedione #
DB-029133
DB-268951
DB-272208
pyrimidine-2,4(1H,3H)-dione, 5-chloro-
CS-0010970
NS00045646
EN300-96343
2(1H)-Pyrimidinone,5-chloro-4-hydroxy-(9ci)
5-Chlorouracil, Vetec(TM) reagent grade, 98%
2(1H)-PYRIMIDINONE, 5-CHLORO-4-HYDROXY-
4(3H)-PYRIMIDINONE, 5-CHLORO-2-HYDROXY-
Q238482
5-chloro-1,2,3,4-tetrahydropyrimidine-2,4-dione
Z1203730752
5UC
Solubility of 5-chloro-1H-pyrimidine-2,4-dione
5-chloro-1H-pyrimidine-2,4-dione, a pyrimidine derivative, exhibits notable solubility characteristics that are of interest in chemical applications. Understanding its solubility is crucial for processes such as reactions, formulations, and pharmaceutical development. Here are key points regarding its solubility:
As one might say, “The solubility of a compound often defines its destiny in chemical pathways.” Therefore, understanding these solubility parameters is vital for leveraging the full potential of 5-chloro-1H-pyrimidine-2,4-dione in both research and industrial contexts.