Interesting facts
Interesting Facts About 2,3-Dibromopropanoic Acid
2,3-Dibromopropanoic acid is an intriguing compound in the field of organic chemistry. Its unique structure and properties make it a subject of interest for both research and educational purposes. Here are several fascinating aspects of this compound:
- Structural Significance: This compound features two bromine atoms attached to a three-carbon chain, specifically at the second and third carbon positions. This arrangement contributes to its distinct reactivity and properties.
- Biochemical Implications: 2,3-Dibromopropanoic acid is often studied for its potential biological activities, including its role as an inhibitor in metabolic pathways. Research suggests that it can affect the metabolism of certain amino acids.
- Synthesis: The synthesis of 2,3-dibromopropanoic acid typically involves the bromination of propanoic acid, highlighting the usefulness of bromination reactions in organic synthesis. This method showcases the utility of halogens in modifying organic compounds.
- Research Applications: Scientists explore this compound for various applications ranging from pharmaceuticals to agricultural chemicals. Its unique properties make it a candidate for developing new derivatives with enhanced biological activity.
- Chirality: The presence of two chiral centers in 2,3-dibromopropanoic acid allows for the existence of multiple stereoisomers. Understanding these variations is crucial in fields like drug development, where the specific orientation of atoms can greatly influence efficacy.
This compound serves as a prime example of how modifications at the molecular level can lead to significant differences in reactivity and application. The study of 2,3-dibromopropanoic acid highlights the intricate balance between structure and function in organic chemistry. As chemists continue to explore its properties, we can anticipate new discoveries that may pave the way for innovative uses in science and technology.
Synonyms
2,3-DIBROMOPROPIONIC ACID
600-05-5
2,3-Dibromopropanoic acid
Propanoic acid, 2,3-dibromo-
Propionic acid, 2,3-dibromo-
alpha,beta-Dibromopropionic acid
NSC 175
UNII-2IIC1DOY4I
2IIC1DOY4I
EINECS 209-981-1
.alpha.,.beta.-Dibromopropionic acid
BRN 1721428
DTXSID3032832
AI3-32762
NSC-175
DTXCID1012832
4-02-00-00767 (Beilstein Handbook Reference)
PROPIONIC ACID, .ALPHA.,.BETA.-DIBROMO-
2,3Dibromopropionic acid
Propanoic acid, 2,3dibromo
Propionic acid, 2,3dibromo
alpha,betaDibromopropionic acid
PROPIONIC ACID, ALPHA,BETA-DIBROMO-
209-981-1
(+-)-2,3-dibromopropionic acid
un3261
zmyaksmztvwujb-uhfffaoysa-n
(+/-)-2,3-DIBROMOPROPIONIC ACID
C3H4Br2O2
2,3-Dibromopropionicacid
MFCD00004212
Propanoic acid,3-dibromo-
Propionic acid,3-dibromo-
2,3-dibromo-propanoic acid
2,3-dibromo-propionic acid
MLS001065610
SCHEMBL511965
NSC175
CHEMBL1399151
2,3-Dibromopropionic acid, 98%
HMS3039J08
Tox21_200140
AKOS009031445
CS-W021482
FD37217
NCGC00091481-01
NCGC00091481-02
NCGC00257694-01
AS-10811
BP-30119
CAS-600-05-5
SMR000568462
DB-053511
D1383
NS00003261
EN300-19715
O10565
Q27254788
F1905-6991
Solubility of 2,3-dibromopropanoic acid
2,3-dibromopropanoic acid, with the chemical formula C3H4Br2O2, exhibits notable solubility characteristics that are important to understand:
Overall, it can be stated that 2,3-dibromopropanoic acid is generally soluble in a range of solvents, which makes it useful in various chemical applications. Such solubility characteristics also make it a subject of interest for further studies in organic chemistry and its derivatives.