2,3-Dibromobutane-1,4-diol
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- Molecular formula
- C4H8Br2O2
- CAS Number
- 34283-63-7
- IUPAC Name
- 2,3-dibromobutane-1,4-diol
- Molecular Weight
- 261.91g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.2800g/cm3
- Appearance
- is characterized by off-white to pale yellow crystalline powder. The compound is known for its crystalline nature and is fairly stable under standard conditions.
- Synonyms
- 2, 3-Dibromo-1, 4-butanediol
Identification
Interesting facts
Interesting Facts about 2,3-Dibromobutane-1,4-diol
2,3-Dibromobutane-1,4-diol is a fascinating compound that belongs to the class of organic halogenated compounds. Here are some key points that highlight its significance:
- Synthesis and Reactions: This compound can be synthesized through the bromination of 1,4-butanediol, a common precursor. The presence of bromine atoms makes it a versatile intermediate in organic synthesis.
- Applications: It has potential applications in pharmaceuticals as a building block for various drug molecules, especially due to its ability to introduce halogen functionality, which is often key to enhancing biological activity.
- Chirality: 2,3-Dibromobutane-1,4-diol exhibits chirality because of the presence of two stereocenters. This property makes it important in the study of stereochemistry and its effects on molecular interactions.
- Biological Relevance: Compounds like 2,3-dibromobutane-1,4-diol are often involved in biological processes, and studying them can provide insights into enzyme mechanisms and metabolic pathways.
- Environmental Impact: As a brominated compound, it is important to consider the environmental implications of its use. Brominated organic compounds can pose challenges in waste management and environmental toxicity.
In summary, 2,3-dibromobutane-1,4-diol serves as an intriguing example of how halogenated compounds play a critical role in organic chemistry, drug development, and understanding stereochemical phenomena. Its synthesis, application in pharmaceuticals, and biological relevance create a rich area for research and discovery.