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2-bromo-N-ethyl-prop-2-en-1-amine

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Identification
Molecular formula
C5H10BrN
CAS number
13404-06-5
IUPAC name
2-bromo-N-ethyl-prop-2-en-1-amine
State
State

The compound is a liquid at room temperature.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
118.00
Boiling point (Kelvin)
391.15
General information
Molecular weight
164.05g/mol
Molar mass
164.0480g/mol
Density
1.3000g/cm3
Appearence

2-bromo-N-ethyl-prop-2-en-1-amine is generally a colorless to pale yellow liquid. It has a distinct odor as typical with many organobromide compounds.

Comment on solubility

Solubility of 2-bromo-N-ethyl-prop-2-en-1-amine

When considering the solubility of 2-bromo-N-ethyl-prop-2-en-1-amine, several factors come into play, primarily influenced by its molecular structure. This compound, featuring both a bromo group and an amine group, exhibits interesting solubility characteristics:

  • Polarity: Due to the presence of the amino group (-NH2), the molecule tends to be polar, which generally enhances solubility in polar solvents like water.
  • Hydrogen Bonding: The amine group can engage in hydrogen bonding, further promoting solubility in water.
  • Bromo Group Influence: The bromo substituent can introduce some hydrophobic character, potentially decreasing solubility in water but may increase solubility in organic solvents.
  • Solvent Interaction: It is often observed that compounds with similar polarity to their solvent will dissolve better; therefore, 2-bromo-N-ethyl-prop-2-en-1-amine could perform well in polar solvents.

In general, the solubility of 2-bromo-N-ethyl-prop-2-en-1-amine can be characterized by a balance: while the amine group promotes solubility in aqueous environments, the bromo group introduces some challenges in terms of solubility in water. Thus, the net solubility may vary based on the solvent used. It is crucial to consider both the chemical environment and the conditions (such as temperature) when evaluating its solubility.

Interesting facts

Interesting Facts about 2-Bromo-N-ethyl-prop-2-en-1-amine

2-Bromo-N-ethyl-prop-2-en-1-amine is a fascinating compound in organic chemistry due to its unique structural features and potential applications. Here are several intriguing aspects:

  • Reactivity: The presence of the bromo group facilitates various nucleophilic substitution reactions, making this compound versatile for creating numerous derivatives.
  • Synthetic Utility: This compound can be employed as a versatile building block in the synthesis of other nitrogen-containing compounds—an essential aspect for drug development.
  • Application in Research: Compounds similar to 2-bromo-N-ethyl-prop-2-en-1-amine are often used in medicinal chemistry research, particularly in the development of potential pharmaceuticals.
  • Involvement in Coupling Reactions: The allylic amine structure allows it to undergo coupling reactions, which can be beneficial in creating complex molecules with high specificity.

In the realm of synthetic organic chemistry, compounds like 2-bromo-N-ethyl-prop-2-en-1-amine are indispensable. They embody the *creativity* that chemists bring to the table, as they can lead to innovative solutions and new materials. As one chemist aptly put it, "In every molecule lies the promise of a new discovery."

Overall, 2-bromo-N-ethyl-prop-2-en-1-amine not only presents engaging challenges for synthesis but also holds significant promise for future applications in various scientific fields.

Synonyms
ALLYLAMINE, 2-BROMO-N-ETHYL-
2-Bromo-N-ethylallylamine
N-(2-Bromoallyl)ethylamine
2-Bromo-N-ethyl-2-propen-1-amine
BRN 1740827
871-23-8
2-Propen-1-amine, 2-bromo-N-ethyl-
DTXSID60236126
4-04-00-01092 (Beilstein Handbook Reference)
DTXCID60158617
2-Propen-1-amine, 2-bromo-N-ethyl-(9CI)
SCHEMBL320773
N-(2-bromo-2-propenyl)-N-ethylamine