Interesting facts
Interesting Facts about 2-Bromobutanoic Acid
2-Bromobutanoic acid is an intriguing compound with various applications in organic chemistry and medicinal research. Below are some fascinating insights about this compound:
- Structural Significance: 2-Bromobutanoic acid features a bromine atom attached to the second carbon of butanoic acid, which introduces unique reactivity patterns that are advantageous in synthesis.
- Reactivity: The presence of the bromine atom makes the compound a valuable intermediate in the synthesis of more complex organic molecules. This allows for:
- Preparation of substituted carboxylic acids
- Formation of amines via bromine displacement reactions
- Biological Importance: Compounds like 2-bromobutanoic acid can act as inhibitors for specific enzyme activities, making them useful in drug development and pharmacological studies. Their structural similarity to natural metabolites allows them to play roles in metabolic pathways.
- Regioselectivity: The compound exemplifies regioselective reactions, where the orientation of reactions can be controlled by the positioning of the bromine atom, providing insight into mechanistic pathways in organic chemistry.
- Research Applications: Ongoing research explores its potential uses in asymmetric synthesis and the development of stereochemically diverse compounds. Scientists often highlight the compound's utility in developing novel therapeutic agents.
As a versatile intermediate, 2-bromobutanoic acid represents the intersection of structural chemistry and medicinal application, making it a noteworthy subject for study in both educational and research settings.
Synonyms
2-BROMOBUTYRIC ACID
2-Bromobutanoic acid
80-58-0
alpha-Bromobutyric acid
Butanoic acid, 2-bromo-
2385-70-8
dl-2-Bromobutyric acid
Butyric acid, 2-bromo-
UNII-MCO6PW23BT
.alpha.-Bromobutyric acid
.alpha.-Bromobytyric acid
MCO6PW23BT
NSC 8024
NSC-8024
EINECS 201-294-5
(+/-)-2-bromobutyric acid
.alpha.-Bromo-n-butyric acid
AI3-52295
Butyric acid, .alpha.-bromo-
DTXSID90861642
DL-.ALPHA.-BROMOBUTYRIC ACID
(+/-)-2-BROMOBUTANOIC ACID
(RS)-.ALPHA.-BROMOBUTYRIC ACID
.ALPHA.-BROMOBUTYRIC ACID [MI]
(+/-)-.ALPHA.-BROMOBUTANOIC ACID
.ALPHA.-BROMOBUTYRIC ACID, (+/-)-
EPA Method 552.3 2-Bromobutanoic Acid 10000 microg/mL in Methyl tert-butyl ether
2-Bromobutanoicacid
Butyric acid, alpha-bromo-
bromobutyric acid
MFCD00210111
MFCD00210112
2Bromobutyric acid
2Bromobutanoic acid
2-bromo-butyric acid
Butyric acid, 2bromo
2-Bromo-butanoic acid
alpha-Bromobytyric acid
Butanoic acid, 2bromo
Butyric acid, alphabromo
WLN: QVYE2
SCHEMBL5323
2-Bromobutyric acid, 97%
Butyric acid, 2bromo (8CI)
DL-ALPHA-BROMOBUTYRIC ACID
DTXCID30219340
NSC8024
BCP24915
HBA65949
(RS)-ALPHA-BROMOBUTYRIC ACID
BBL011564
MFCD00004216
STL146735
AKOS000118937
AKOS016039402
CS-W016049
HY-W015333
SB46762
SB46765
(+/-)-ALPHA-BROMOBUTANOIC ACID
DA-19660
SY233332
SY233336
VS-02981
ALPHA-BROMOBUTYRIC ACID, (+/-)-
DB-016188
DB-056449
B0564
NS00041015
EN300-19244
Q209315
F2191-0227
Solubility of 2-bromobutanoic acid
2-bromobutanoic acid, with the chemical formula C4H7BrO2, exhibits notable characteristics in its solubility behavior. As a carboxylic acid, it tends to dissolve readily in polar solvents, particularly in:
However, its solubility may be influenced by temperature and concentration:
What is particularly interesting is the compound's structural effect on solubility. The presence of the bromine atom affects not only the polarity but also introduces steric hindrance, which can impact the overall solubility in various solvents.
It is essential to consider these factors when predicting the solubility profile of 2-bromobutanoic acid in different chemical environments.