Interesting facts
Interesting Facts about 1-Bromo-2-methyl-butane
1-Bromo-2-methyl-butane is an intriguing compound that finds its place within the realm of organic chemistry. As a member of the alkyl halides, this compound exhibits unique chemical properties and reactivity that can lead to fascinating experiments and applications. Here are some noteworthy aspects of 1-bromo-2-methyl-butane:
- Structure and Isomerism: This compound features a branched alkyl chain, which leads to its classification as a secondary bromoalkane. The presence of the bromine atom introduces significant potential for nucleophilic substitution reactions, allowing for various synthetic pathways.
- Reactivity: As an alkyl halide, 1-bromo-2-methyl-butane is particularly reactive towards nucleophiles. Its reactivity patterns can be explored through both SN1 and SN2 mechanisms, making it a valuable model compound for studying reaction kinetics and mechanisms.
- Synthetic Applications: This compound can serve as an intermediate in the synthesis of more complex organic molecules. It has applications in pharmaceuticals and agrochemicals, showcasing its importance in industrial chemistry.
- Chiral Center Potential: Although 1-bromo-2-methyl-butane itself is not chiral, it can be transformed into chiral compounds. Understanding these transformations can aid in chiral resolution studies, a key aspect in the development of drug molecules.
- Environmental Impact: Like many halogenated compounds, 1-bromo-2-methyl-butane must be handled with care due to its potential environmental and health impacts. This reinforces the importance of studying organic compounds with respect to sustainability and safety.
In summary, 1-bromo-2-methyl-butane is not just a simple alkyl halide; it opens a gateway to numerous discussions in chemistry, ranging from reaction mechanisms to environmental considerations. Its diverse applications and reactivity make it a fascinating subject for study in both academic and industrial settings.
Synonyms
1-BROMO-2-METHYLBUTANE
10422-35-2
Butane, 1-bromo-2-methyl-
5973-11-5
2-Methylbutyl Bromide
1-bromoisopentane
DL-1-Bromo-2-methylbutane
(1)-1-Bromo-2-methylbutane
9787127K0P
DTXSID50870593
UNII-9787127K0P
2-METHYLBUTAN-1-YL BROMIDE
Butane, 1-bromo-2-methyl-, DL-
EINECS 227-768-1
Butane, 1-bromo-2-methyl-, (.+/-.)-
DTXCID20818301
Butane, 1-bromo-2-methyl-, (+-)-
1-BROMO-2-METHYLBUTANE, (+-)-
227-768-1
600-538-1
xkvlzbnepalhio-uhfffaoysa-n
1-Bromo-2-methyl-butane
MFCD00000218
(+)-2-Methylbutyl bromide
1-Bromo-2-methyl butane
2-methylbromobutane
2-methyl-1-bromobutane
1-Bromo 2 methylbutane
1-bromo--2-methylbutane
(+)-2-methylbutylbromide
d-1-Bromo-2-methylbutane
(+) 2-methylbutyl bromide
1-bromanyl-2-methyl-butane
SCHEMBL115533
CHEMBL156329
SCHEMBL1129887
SCHEMBL7873050
SCHEMBL27825972
(+/-)-1-bromo-2-methyl butane
SBB007669
AKOS009158562
(+-) 1-BROMO-2-METHYLBUTANE
AS-44338
1-BROMO-2-METHYLBUTANE, (+/-)-
DB-080873
DB-361789
NS00081740
A10884
EN300-125818
A800932
Q27271981
Solubility of 1-bromo-2-methyl-butane (C5H11Br)
1-bromo-2-methyl-butane, a member of the alkyl halides, has distinctive solubility characteristics that are essential to understand. Being an organic compound with a relatively large hydrophobic hydrocarbon chain and a polar bromo group, its solubility reflects a balance between these two structural components.
Key Points on Solubility:
In summary, while 1-bromo-2-methyl-butane has some solubility in organic solvents, its hydrophobic nature results in a diminished capacity for aqueous solubility. Understanding these solubility traits is crucial for effective application and handling in chemical processes.