Interesting facts
Interesting Facts about Pyrimidin-2-amine
Pyrimidin-2-amine is a fascinating compound that belongs to the class of heterocyclic aromatic amines. This compound plays a significant role in various fields of chemistry and biochemistry. Here are some intriguing aspects:
- Structural Importance: Pyrimidin-2-amine has a pyrimidine ring that serves as a crucial building block in the synthesis of several important compounds, including pharmaceuticals and agrochemicals.
- Biological Activity: This compound is often researched for its potential biological activities. It has been studied for its ability to inhibit specific enzymes, which could lead to the development of novel therapeutics.
- Versatile Precursor: Pyrimidin-2-amine can be used as a precursor in the synthesis of nucleobases and other nitrogen-containing heterocycles, essential components of nucleic acids. This highlights its significance in molecular biology.
- Research Applications: Scientists have examined pyrimidin-2-amine for its anti-cancer, anti-viral, and anti-inflammatory properties, making this compound of high interest in medicinal chemistry.
- Derivative Development: The modification of pyrimidin-2-amine leads to a variety of derivatives, each with distinct properties and potential applications in drug design and molecular research.
In conclusion, pyrimidin-2-amine is not just a simple heterocyclic compound; it is a vital player in the ongoing quest for new medicinal agents and plays a fundamental role in biochemical research. As stated by renowned chemist Robert H. Grubbs, "The beauty of chemistry lies in the connections we forge through our understanding of compounds like pyrimidin-2-amine."
Synonyms
2-AMINOPYRIMIDINE
pyrimidin-2-amine
109-12-6
2-Pyrimidinamine
Aminopyrimidine
Pyrimidin-2-ylamine
2-Pyrimidiylamine
Pyrimidine, 2-amino-
2-Pyridiylamine
1,2-Dihydro-2-iminopyrimidine
2-amino-pyrimidine
NSC 1912
EINECS 203-648-4
Pyrimidinamine
OB8I17P2G4
2(1H)-Pyrimidinimine (9CI)
153824-54-5
CHEBI:38618
AI3-24128
NSC-1912
Pyrimidine, 1,2-dihydro-2-imine-
MFCD00006089
2(1H)-Pyrimidinimine, (E)- (9CI)
2(1H)-Pyrimidinimine, (Z)- (9CI)
CHEMBL88580
DTXSID70870459
176773-04-9
176773-05-0
PYRIMIDINE, 1,2-DIHYDRO-2-IMINO-
SULFADIAZINE IMPURITY A [EP IMPURITY]
551920-04-8
amino pyrimidine
SULFADIAZINE IMPURITY A (EP IMPURITY)
iminopyrimidine
pyrimidyl amine
2Pyrimidinamine
amino-pyrimidine
2Pyrimidiylamine
Pyrimidin2ylamine
2-Aminpirimidina
2-aminopirimidina
Pyrimidin-2-amine; Sulfadiazine Imp. A (Pharmeuropa); Sulfadiazine Impurity A
2-amino pyrimidine
pyrimidine-2-amine
LGA
Pyrimidine, 2amino
pyrimidin-2-yl-amine
27043-39-6
Sulfadiazine Impurity A
2-Aminopyrimidine, 97%
1,2Dihydro2iminopyrimidine
UNII-OB8I17P2G4
Pyrimidine, 1,2dihydro2imino
DTXCID40818181
NSC1912
BDBM50354823
STK317800
AKOS000119323
Pyrimidine, 1,2dihydro2imino (7CI)
CS-W020110
FA34676
MB00175
AC-15596
AS-13594
HY-41340
Pyrimidine, 1,2-dihydro-2-imine-(7CI)
DB-015939
DB-347327
A0412
NS00004461
EN300-17309
2-Aminopyrimidine, Vetec(TM) reagent grade, 97%
A801969
Q27117919
F3329-0410
Sulfadiazine impurity A, European Pharmacopoeia (EP) Reference Standard
203-648-4
Solubility of Pyrimidin-2-amine
Pyrimidin-2-amine, known for its aromatic ring structure, exhibits intriguing solubility characteristics that can vary significantly based on the solvent used. This compound is generally considered to be:
It is essential to highlight that the solubility of pyrimidin-2-amine can be influenced by several factors, including temperature and pH of the solution. For instance:
Overall, understanding the solubility of pyrimidin-2-amine is crucial for its applications in medicinal chemistry and various synthetic processes, as it affects the compound's reactivity and bioavailability.