Interesting facts
Interesting Facts about 2-bromo-3-methyl-butanoic Acid
2-bromo-3-methyl-butanoic acid is a fascinating compound in the realm of organic chemistry, primarily due to its structural features and applications. Here are some intriguing aspects worth noting:
- Structural Significance: This compound is a member of the branched-chain carboxylic acids and features both a bromine atom and a methyl group attached to its carbon chain. This unique structure allows it to exhibit interesting reactivity, making it a target for synthetic chemists.
- Reagent for Synthesis: 2-bromo-3-methyl-butanoic acid often acts as a useful reagent in organic synthesis. It plays a vital role in the preparation of other compounds, particularly in the creation of amino acids and other biologically significant molecules.
- Biological Relevance: This acid is significant in studies related to metabolic pathways and can be utilized to investigate the effects of various substituents on biological activity. Its derivatives may have applications in pharmaceutical research.
- Chirality: The presence of four different groups attached to its chiral center allows for the existence of enantiomers. This property is crucial in the development of drug compounds, as different enantiomers can exhibit dramatically different biological effects.
- Applications in Research: Beyond its role as a synthetic intermediate, this compound has been explored in various academic research settings, contributing to the understanding of reaction mechanisms and the principles of stereochemistry.
In conclusion, 2-bromo-3-methyl-butanoic acid is more than just a chemical; it's a window into the complexity of organic synthesis and biological interactions. As emphasized by chemists, “Understanding the subtleties of structure can lead to groundbreaking discoveries.” Its unique features continue to make it a subject of interest in various scientific fields.
Synonyms
2-Bromo-3-methylbutyric acid
565-74-2
2-Bromo-3-methylbutanoic acid
2-Bromoisovaleric acid
Butanoic acid, 2-bromo-3-methyl-
alpha-Bromoisovaleric acid
Butyric acid, 2-bromo-3-methyl-
NSC 167
.alpha.-Bromoisovaleric acid
EINECS 209-291-0
BRN 1721146
M69LGV465C
AI3-21065
NSC-167
NSC-6967
DTXSID30870617
.ALPHA.-BROMOISOVALERIC ACID [MI]
DL-.ALPHA.-BROMO-.BETA.-METHYLBUTYRIC ACID
DTXCID70223305
DL-ALPHA-BROMO-BETA-METHYLBUTYRIC ACID
209-291-0
(+-)-.alpha.-bromoisopentanoic acid
(+-)-alpha-bromoisopentanoic acid
inchi=1/c5h9bro2/c1-3(2)4(6)5(7)8/h3-4h,1-2h3,(h,7,8
2-Bromo-3-methylbutyricacid
169320-29-0
(+/-)-.ALPHA.-BROMOISOPENTANOIC ACID
(+/-)-2-BROMO-3-METHYLBUTYRIC ACID
a-Bromoisovaleric Acid
UNII-M69LGV465C
S-2-Bromo-3-methyl-butyric acid
Bromisovaleriansaure
MFCD00004210
|A-Bromoisovaleric acid
alpha-bromo-isovaleric acid
SCHEMBL659682
2-bromo-3-methyl-butyric acid
NSC167
Isovaleric acid, .alpha.-bromo-
NSC6967
BBL010942
STK802038
2-Bromo-3-methylbutyric acid, 97%
AKOS000121095
AKOS022060511
FB38473
SB44751
SB47853
AS-11032
SY033749
(+/-)-ALPHA-BROMOISOPENTANOIC ACID
DB-013638
DB-020607
B0668
CS-0498321
NS00042359
EN300-25402
A10761
alpha-Bromoisovaleric acid, purum, >=98.0% (GC)
Q27283553
Z203888738
Solubility of 2-bromo-3-methyl-butanoic acid
2-bromo-3-methyl-butanoic acid, with the chemical formula C5H9BrO2, displays interesting solubility properties that are influenced by its molecular structure. Generally, acidic compounds such as carboxylic acids have varying solubility in water depending on:
In summary, while 2-bromo-3-methyl-butanoic acid is likely to be soluble in water due to its polar carboxylic group, the overall solubility can be impacted by its hydrophobic characteristics and temperature variations. As a rule of thumb, “like dissolves like” applies here; thus, understanding the balance of polar and non-polar features is key to predicting its solubility behavior.