Interesting facts
Interesting Facts about 2,3-Dibromopropan-1-ol
2,3-Dibromopropan-1-ol is a fascinating chemical compound with multiple applications and intriguing properties that engage both chemists and students alike. This compound belongs to the family of alcohols and halogenated hydrocarbons. Here are some interesting aspects:
- Reactivity: 2,3-Dibromopropan-1-ol is known for its reactivity in organic synthesis. It can undergo various reactions, such as substitution and elimination, making it a valuable intermediate in the synthesis of more complex organic molecules.
- Use in Research: It often serves as a precursor in the creation of other compounds, particularly in medicinal chemistry, where the bromine atoms can influence the biological activity of the final products.
- Biological Implications: Understanding the structure and reactivity of 2,3-dibromopropan-1-ol can provide insights into how halogenated compounds interact with biological systems, which is crucial for drug development.
- Chirality: This compound features stereocenters, leading to the possibility of existing in multiple stereoisomeric forms. Chirality plays a significant role in pharmacology; different enantiomers can exhibit vastly different effects in biological systems.
- Historical Significance: Halogenated alcohols like 2,3-dibromopropan-1-ol have historical significance in the study of organic chemistry and the development of early synthetic methods, pushing the boundaries of chemical science.
In summary, 2,3-dibromopropan-1-ol is not merely a chemical entity; it opens doors to a wide range of studies in organic synthesis and biological interactions. Its unique properties make it a topic of interest in both academic and industrial settings, encouraging further investigation into its potential applications.
Synonyms
2,3-Dibromo-1-propanol
96-13-9
2,3-Dibromopropan-1-ol
2,3-DIBROMOPROPANOL
Dibromopropanol
1-Propanol, 2,3-dibromo-
Brominex 257
2,3-Dibromopropyl alcohol
1,2-Dibromopropan-3-ol
USAF DO-42
DBP (flame retardant)
NCI-C55436
CCRIS 940
HSDB 2879
UNII-C0YBW1OA2I
C0YBW1OA2I
2,3-dibromo-propan-1-ol
NSC 6203
EINECS 202-480-9
1,2-Dibromohydrin
BRN 1719127
DTXSID7021817
AI3-26304
NSC-6203
DTXCID801817
NSC6203
Brominex 257; DBP; NSC 6203
2,3-DIBROMOPROPAN-1-OL [HSDB]
C3H6Br2O
beta-Dibromohydrin
Allyl alcohol dibromide
Glycerol 1,2-dibromohydrin
MFCD00004699
.beta.-Dibromohydrin
1,2Dibromopropan3ol
2,3Dibromo1propanol
alpha,beta-Dibromohydrin
1-Propanol,3-dibromo-
1Propanol, 2,3dibromo
2,3Dibromopropyl alcohol
WLN: Q1YE1E
MLS002415682
SCHEMBL288971
CHEMBL1403428
CHEBI:19310
Glycerol alpha,beta-Dibromohydrin
2 pound not3-Dibromo-1-propanol
2,3-Dibromo-1-propanol, 98%
HMS3039C16
Tox21_200709
STL301889
AKOS009157161
CAS-96-13-9
NCGC00091310-01
NCGC00091310-02
NCGC00258263-01
SMR001370876
DB-057622
D0204
NS00009283
C19224
E76987
Q26840749
Solubility of 2,3-dibromopropan-1-ol
2,3-dibromopropan-1-ol, with the chemical formula C3H6Br2O, is a compound of notable interest when discussing solubility. The presence of both hydroxyl (-OH) and bromine (Br) functional groups in its structure significantly influences its solubility characteristics.
Key Factors Affecting Solubility:
Overall, 2,3-dibromopropan-1-ol is expected to be soluble in water due to its combination of polar functional groups. However, it may have limited solubility in non-polar solvents due to the presence of the hydrophilic –OH group, which prefers interaction with polar molecules. This balance of interactions illustrates the fascinating complexities of solubility in chemical compounds.