Interesting facts
Interesting Facts about 8-Bromo-1,3-Dimethyl-7H-Purine-2,6-Dione
8-Bromo-1,3-dimethyl-7H-purine-2,6-dione, also known as 8-bromo-AD, is a fascinating compound primarily studied for its role in biochemistry and potential pharmaceutical applications. Below are some intriguing details that may pique the interest of both chemists and biochemists alike:
- Structural Characteristics: This compound belongs to the class of purines, which are significant for their role as foundational building blocks of nucleic acids like DNA and RNA. Its unique structure includes a bromine atom, which can influence its biological activity and interactions.
- Biological Significance: 8-Bromo-1,3-dimethyl-7H-purine-2,6-dione has been studied for its potential effects on various biological pathways, including those related to metabolic processes and cellular signal transduction.
- Pharmacological Potential: Research indicates that compounds like this one may possess therapeutic properties, including anti-inflammatory and antioxidant effects, making them a focus for drug design and development.
- Synthesis: The synthesis of purine derivatives is an essential area of study. Researchers frequently explore different methodologies to obtain 8-bromo-1,3-dimethyl-7H-purine-2,6-dione, optimizing yields and purity.
- Research Application: Because of its unique properties, this compound is utilized in biochemical assays and research settings to explore cellular responses and molecular interactions.
In summary, 8-bromo-1,3-dimethyl-7H-purine-2,6-dione is not only a valuable compound in the realm of synthetic organic chemistry but also a significant substance in biological research. Its special characteristics continue to inspire scientific inquiry and development.
Synonyms
Bromotheophylline
Theophylline, 8-bromo-
1H-Purine-2,6-dione, 8-bromo-3,7-dihydro-1,3-dimethyl-
UNII-FZG87K1MQ6
FZG87K1MQ6
EINECS 233-846-6
NSC 164940
NSC-164940
8-BROMOTHEOPHYLLINE (USP-RS)
8-BROMOTHEOPHYLLINE [USP-RS]
8-Bromotheophylline
10381-75-6
8-Bromo-1,3-dimethyl-1H-purine-2,6(3H,9H)-dione
8-bromo-1,3-dimethyl-7H-purine-2,6-dione
8-bromo-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione
8-bromo-1,3-dimethyl-3,9-dihydro-1H-purine-2,6-dione
8-Bromotheophyline
8-bromo-1,3-dimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione
CHEMBL316160
DTXSID7044768
MFCD00022664
8-bromo-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione
8-Bromo-1,3-dimethyl-3,7-dihydro-purine-2,6-dione
NCGC00167564-01
1H-Purine-2,6-dione, 8-bromo-3,9-dihydro-1,3-dimethyl-
DTXCID5024768
C7H7BrN4O2
CAS-10381-75-6
8-bromo-theophylline
MFCD01848460
Oprea1_299436
Oprea1_509676
MLS004754491
SCHEMBL237881
8-Bromotheophylline (Standard)
HY-W088152R
Tox21_112559
BBL012666
BDBM50045345
CCG-19376
NSC164940
STK803299
AKOS000274376
AKOS001283003
Tox21_112559_1
DB14018
FB09836
GS-5727
HY-W088152
8-bromo-1,3-dimethylpurine-2,6-dione
NCGC00167564-03
NCGC00167564-04
SMR002397689
SY023545
DB-040487
8-bromo-6-hydroxy-1,3-dimethylpurin-2-one
B3456
CS-0130336
NS00023263
EN300-17892
H10528
SBI-0653938.0001
AB01300038-01
AB01300038_03
AF-399/37411012
SR-01000479300
1H-Purine-2, 8-bromo-3,7-dihydro-1,3-dimethyl-
8-BROMO-1,3-DIMETHYL-9H-PURINE-2,6-DIONE
SR-01000479300-1
Q27278353
Z57161790
8-bromo-1,3-dimethyl-1H-purine-2,6(3H, 7H)-dione
F0807-0406
Solubility of 8-bromo-1,3-dimethyl-7H-purine-2,6-dione
When examining the solubility of 8-bromo-1,3-dimethyl-7H-purine-2,6-dione, several factors come into play:
As a general rule, compounds that can form hydrogen bonds tend to have higher solubility in polar solvents. However, the presence of the bromine atom could hinder solubility in certain environments due to its larger size and varying electronegativity compared to carbon and hydrogen. Therefore, while 8-bromo-1,3-dimethyl-7H-purine-2,6-dione may exhibit moderate solubility in water, solubility may also significantly depend on other factors including:
In conclusion, the solubility of 8-bromo-1,3-dimethyl-7H-purine-2,6-dione is influenced by its molecular structure and interactions with the solvent, making it essential to consider both the chemical environment and method of preparation when evaluating its dissolvability in various solvents.