Interesting facts
Exploring 2,3-Dibromobutane
2,3-Dibromobutane is an intriguing compound in the field of organic chemistry, notable for its role in both synthetic applications and its structural characteristics. Here are some fascinating facts about this compound:
- Stereo Isomerism: 2,3-Dibromobutane can exist as different stereoisomers. Specifically, it has two enantiomers, which are mirror images of each other. This property is crucial in organic synthesis, especially in asymmetric synthesis, where the chirality of molecules can significantly influence their biological activity.
- Reactivity: The presence of bromine atoms makes this compound quite reactive. For instance, it can undergo nucleophilic substitution reactions, which are pivotal in forming various derivatives and other complex organic molecules. The bromine atoms are excellent leaving groups, making the compound an excellent candidate for further transformations.
- Applications: 2,3-Dibromobutane is used in synthetic organic chemistry and can serve as a precursor to more complex molecules. It's often utilized in research to study reaction mechanisms and stereochemistry, providing invaluable insights into the behavior of organic compounds.
- Natural Occurrence: Although 2,3-dibromobutane is primarily synthesized in labs, compounds with similar structures can also be found in nature, where halogenated compounds play crucial roles in ecology and biological processes.
- Historical Significance: The study of brominated compounds like 2,3-dibromobutane has contributed significantly to the development of synthetic organic chemistry. Historically, understanding these compounds has paved the way for advances in pharmaceuticals and agrochemicals.
In summary, the study of 2,3-dibromobutane is not only vital in academic research but also opens up numerous possibilities in the development of new materials and medicines. As one delves deeper into the chemistry of this compound, one uncovers layers of complexity and potential, showcasing how a simple structure can lead to profound scientific discoveries.
Synonyms
2,3-DIBROMOBUTANE
5408-86-6
Butane, 2,3-dibromo-
NSC 8414
EINECS 226-476-1
DTXSID70871128
Butane, 2,3dibromo
DTXCID60818800
226-476-1
598-71-0
(+/-)-2,3-Dibromobutane
dl-2,3-Dibromobutane
MFCD00000146
dibromo butane
rel-(2S,3S)-2,3-dibromobutane
(.+-.)-2,3-Dibromobutane
NSC8414
Butane,3-dibromo-
(R*,R*)-(+-)-2,3-Dibromobutane
starbld0004331
.beta.-Butylene bromide
Butane, 2,3-dibromo-, (R*,R*)-(+-)-
Butane,3-dibromo-, meso-
SCHEMBL1668124
Butane,3-dibromo-, (.+-.)-
Butane,3-dibromo-, (R*,S*)-
FAA40886
NSC-8414
NSC115796
NSC245048
STL264217
(+/-)-2,3-Dibromobutane, 98%
2,3-Dibromobutane, (+/-) + meso
AKOS015913326
CS-W014879
NSC 245048
NSC-115796
NSC-245048
AS-10545
SY029617
DB-052476
D0177
NS00043165
Butane,3-dibromo-, (R*,R*)-(.+-.)-
D89609
EN300-124518
F0001-1420
InChI=1/C4H8Br2/c1-3(5)4(2)6/h3-4H,1-2H
Solubility of 2,3-Dibromobutane
2,3-Dibromobutane (C4H8Br2) is an intriguing organic compound with distinct solubility characteristics. This molecule is a dibrominated derivative of butane, and its solubility behavior can be understood by considering several key factors:
In summary, the solubility of 2,3-dibromobutane is markedly dependent on the type of solvent used. Its relatively low solubility in water can be summarized with the phrase: "Like dissolves like." This serves as a reminder of the crucial role polarity plays in the solubility of chemical compounds.