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1,3-Dibromopropan-2-ol

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Identification
Molecular formula
C3H6Br2O
CAS number
96-13-9
IUPAC name
1,3-dibromopropan-2-ol
State
State

At room temperature, 1,3-Dibromopropan-2-ol is typically a liquid. Its chemical characteristics allow it to remain in a liquid state under standard conditions of temperature and pressure.

Melting point (Celsius)
44.00
Melting point (Kelvin)
317.15
Boiling point (Celsius)
236.00
Boiling point (Kelvin)
509.15
General information
Molecular weight
219.89g/mol
Molar mass
219.9220g/mol
Density
2.1390g/cm3
Appearence

1,3-Dibromopropan-2-ol appears as a colorless to light-yellow liquid. It may exhibit a slightly viscous consistency due to the presence of hydroxyl and bromine groups in its structure. The compound might also be slightly odorous, denoting its organic nature and halogen content.

Comment on solubility

Solubility of 1,3-Dibromopropan-2-ol

1,3-Dibromopropan-2-ol, with the chemical formula C3H6Br2O, exhibits unique solubility characteristics due to its molecular structure. Here’s what you need to know:

  • Polar Nature: The presence of the hydroxyl group (-OH) makes 1,3-dibromopropan-2-ol polar, allowing it to interact favorably with polar solvents.
  • Solvent Interaction: This compound is typically soluble in water and other polar solvents, as well as in organic solvents like ethanol and methanol.
  • Hydrophobic Interactions: Despite its polar nature, the bromine substituents introduce some hydrophobic character, which may limit solubility in less polar solvents.

In summary, 1,3-dibromopropan-2-ol is soluble primarily in polar solvents, making it useful in various chemical applications where solubility is a critical factor. As a general rule, remember that like dissolves like: polar compounds mix well with polar solvents, while non-polar compounds do not.

Interesting facts

Interesting Facts About 1,3-Dibromopropan-2-ol

1,3-Dibromopropan-2-ol is a compelling compound that demonstrates the fascinating interplay of halogenation and alcohol function. This specific organic molecule has garnered attention for various reasons:

  • Application in Organic Synthesis: This compound serves as a versatile intermediate in organic synthesis. Its structure allows for multiple pathways for further reactions, making it a valuable building block in chemical synthesis.
  • Studied for Its Biological Activity: 1,3-Dibromopropan-2-ol is of interest in medicinal chemistry due to its potential biological properties. Researchers are investigating its effects as a potential antimicrobial or antifungal agent.
  • Halogen Chemistry: The presence of bromine atoms introduces distinctive reactivity patterns. Compounds like 1,3-dibromopropan-2-ol exemplify the significance of halogens in organic chemistry and their ability to participate in nucleophilic substitution reactions.
  • Chiral Centers: This compound possesses a chiral center, making it interesting in the context of stereochemistry. Understanding its optical activity and how it interacts with plane-polarized light can lead to insights about its enantiomers and their chemical behavior.

As a molecule featuring a combination of alcohol and halogen functionalities, 1,3-dibromopropan-2-ol captivates both theoretical and practical chemists. As stated by a renowned chemist, "The beauty of organic chemistry lies in the myriad of transformations that simple compounds can undergo, revealing complex structures and properties."

Overall, 1,3-dibromopropan-2-ol stands as a noteworthy compound in organic chemistry, opening doors to research and synthesis that deepen our understanding of chemical reactivity and functional applications.

Synonyms
1,3-Dibromo-2-propanol
1,3-Dibromopropan-2-ol
96-21-9
2-Propanol, 1,3-dibromo-
1,3-Dibromohydrin
Glycerol 1,3-dibromohydrin
2-Hydroxy-1,3-dibromopropane
.alpha.-Dibromohydrin
1,3-DIBROMO-2-HYDROXYPROPANE
alpha-Dibromohydrin
NSC 636
1,3-Dibromopropanol
.alpha.,.gamma.-Dibromohydrin
Glycerol alpha,gamma-dibromohydrin
Glycerol alpha,gamma-dibromohydrine
Glycerol-alpha,gamma-dibromohydrine
EINECS 202-489-8
4L2X3X1FPT
Glycerol .alpha.,.gamma.-dibromohydrin
BRN 1732074
NSC-636
MFCD00000216
UNII-4L2X3X1FPT
1,3-dibromo-propan-2-ol
Glycerol .alpha.,.gamma.-dibromohydrine
DTXSID8059130
4-01-00-01496 (Beilstein Handbook Reference)
DIBROMO-2-PROPANOL, 1,3-
2-Propanol,3-dibromo-
alpha,gamma-Dibromohydrin
1.3-Dibromo-2-propanol
alpha,alpha'-Dibromohydrin
WLN: E1YQ1E
SCHEMBL39040
1,3-dibromo-2-propylalcohol
NSC636
DTXCID9048980
1,3-DBP
Glycerol alpha,alpha'-Dibromohydrin
AAA09621
STR07916
AKOS016010338
CS-W014808
SY012889
DB-057629
D0187
NS00040476
EN300-120032
1,3-Dibromo-2-propanol, technical grade, 95%
1,3-Dibromo-2-propanol (stabilized with Copper chip)
Q27893167
methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4-hy