Interesting facts
Interesting Facts about 1,3-Dichlorobutane
1,3-Dichlorobutane is an interesting compound in the realm of organic chemistry, primarily known for its versatile applications and unique properties. Here are some fascinating insights into this dichlorinated alkane:
- Structure and Isomerism: The molecular structure of 1,3-dichlorobutane features two chlorine atoms attached to the first and third carbon atoms of a butane chain. This arrangement allows it to exist as different isomers, such as 1,2-dichlorobutane and 2,3-dichlorobutane, showcasing the importance of *stereochemistry* in determining the compound's behavior.
- Reactivity: The presence of two chlorine atoms enhances the reactivity of 1,3-dichlorobutane. It can undergo multiple types of reactions, including nucleophilic substitutions and elimination reactions, making it a valuable intermediate in organic synthesis.
- Applications: 1,3-Dichlorobutane is used in the synthesis of various organic compounds, particularly in the production of agrochemicals and pharmaceuticals. Its unique properties make it a precursor for developing targeted molecules in chemical research.
- Environmental Considerations: As a chlorinated compound, 1,3-dichlorobutane poses questions about environmental impact and toxicity. Understanding its behavior in biological systems and the environment is essential for assessing its safety and regulatory measures.
- Laboratory Studies: In laboratory settings, 1,3-dichlorobutane serves as a common solvent for reactions involving nonpolar compounds, making it a valuable resource for chemists working with hydrophobic substances.
As one delves into the world of organic chemistry, the study of compounds like 1,3-dichlorobutane not only illuminates complex chemical processes but also emphasizes the interconnectedness of structure, reactivity, and application in scientific innovations. This compound exemplifies how *even small chemical changes can lead to significant alterations in properties and functions*.
Synonyms
1,3-DICHLOROBUTANE
Butane, 1,3-dichloro-
1190-22-3
EINECS 214-718-9
DTXSID90870855
Butane, 1,3dichloro
DTXCID30818539
214-718-9
qbgvarbiqghvkr-uhfffaoysa-n
un1993
1,3-Dichloro-butane
MFCD00000870
1,3-Dichlorobutane, 99%
SCHEMBL162994
CHEMBL352037
AKOS006221689
BS-43853
CS-0442069
D0348
NS00042734
D89632
Solubility of 1,3-Dichlorobutane
1,3-Dichlorobutane, with the chemical formula C4H8Cl2, exhibits unique solubility characteristics primarily due to its molecular structure. Its properties can be summarized as follows:
In conclusion, the solubility of 1,3-Dichlorobutane is significantly influenced by its dual chlorination and hydrocarbon backbone, making it preferentially soluble in non-polar solvents and poorly soluble in polar solvents such as water. As with many organic compounds, understanding these solubility patterns can offer crucial insights into their behavior in various chemical environments.