1-bromo-N-tert-butyl-N,3-dimethylbutan-2-amine

Identification

Molecular formula

C₁₀H₂₂BrN

CAS number

null

IUPAC name

1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine

State

At room temperature, this compound is generally in a liquid state.

Melting point (Celsius)

-65.00

Melting point (Kelvin)

208.15

Boiling point (Celsius)

163.20

Boiling point (Kelvin)

436.35

General information

Molecular weight

207.13g/mol

Molar mass

207.1320g/mol

Density

0.8123g/cm³

Appearence

The compound is typically a colorless to pale yellow liquid.

Comment on solubility

Solubility of 1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine

The solubility of 1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine can be influenced by several factors, including its molecular structure and the nature of the solvent. This compound, featuring both a bromine atom and a tert-butyl group, tends to display interesting solubility characteristics, particularly in organic solvents. Here are some key points to consider:

Polar and non-polar interactions: The presence of the bromine atom indicates a degree of polarity, which can promote solubility in polar solvents like alcohols and acetone.
Hydrophobic character: The tert-butyl moiety increases the hydrophobicity of the compound, often leading to enhanced solubility in non-polar solvents such as hexane and dichloromethane.
Solvent effects: Due to the steric hindrance from the bulky tert-butyl group, the solubility in water is likely to be low; however, solubility might improve in mixtures of water and organic solvents.
Functional implications: The overall solubility profile may play a significant role in the compound's reactivity and applications, making it essential to understand how it interacts with specific solvent systems.

In summary, while 1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine is expected to be more soluble in organic solvents due to its structural features, its solubility in aqueous environments is probably limited. Understanding these solubility parameters is crucial for its practical applications in chemical processes.

Interesting facts

Interesting Facts about 1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine

1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine, commonly referred to in the scientific community as a brominated amine, is notable for its structural complexity and unique properties. As a member of the class of compounds known as amines, it has a variety of chemical behaviors and applications.

Key Characteristics

Structure: The presence of both a tert-butyl group and a bromine atom makes this compound particularly interesting for synthetic applications in organic chemistry.
Reactivity: The bromine atom can serve as a good leaving group, facilitating nucleophilic substitution reactions. This feature is especially valuable in the creation of more complex molecules.
Applications: Due to its unique characteristics, it may be utilized in various fields, including pharmaceuticals and agrochemicals, often as an intermediate in the synthesis of more complex structures.

Scientific Insights

When working with 1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine, researchers often explore its reactivity patterns. Understanding these can lead to the development of novel synthetic pathways. Furthermore, this compound can be a model for studying steric hindrance due to the bulky tert-butyl group, impacting how it interacts with other molecules.

In conclusion, the exploration of 1-bromo-N-tert-butyl-N,3-dimethyl-butan-2-amine is a thrilling aspect of organic chemistry that embodies the creativity and complexity of chemical synthesis. As one delves deeper into its properties and applications, the potential for discovering new chemical behaviors and reactions becomes apparent, marking its significance in advancing the field.