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Climazolam

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Identification
Molecular formula
C6H14ClN
CAS number
3564-74-3
IUPAC name
N-chloro-N-isopropyl-propan-2-amine
State
State

At room temperature, N-chloro-N-isopropyl-propan-2-amine is generally present as a liquid.

Melting point (Celsius)
-57.00
Melting point (Kelvin)
216.15
Boiling point (Celsius)
65.00
Boiling point (Kelvin)
338.15
General information
Molecular weight
109.64g/mol
Molar mass
109.5640g/mol
Density
0.9124g/cm3
Appearence

N-chloro-N-isopropyl-propan-2-amine typically appears as a colorless to pale yellow liquid. It can also have a faint amine-like odor associated with it.

Comment on solubility

Solubility of N-chloro-N-isopropyl-propan-2-amine

N-chloro-N-isopropyl-propan-2-amine, a derivative of amine, exhibits unique solubility characteristics that are of interest in various applications. Its solubility can be influenced by several factors:

  • Polarity: The presence of the chlorine atom imparts a level of polarity to the molecule, which can enhance solubility in polar solvents, such as water.
  • Hydrophobicity: The isopropyl group introduces hydrophobic characteristics, which may limit solubility in aqueous environments.
  • Temperature Effects: Increasing temperature often increases solubility; thus, this compound may dissolve better in warm solvents.

Furthermore, it's important to note that:

  • "Like dissolves like": Solubility is generally higher when the solvent and solute share similar chemical properties.
  • In many cases, N-chloro-N-isopropyl-propan-2-amine may be more soluble in organic solvents such as ethanol or acetone compared to its solubility in water.

Overall, understanding the solubility of N-chloro-N-isopropyl-propan-2-amine is crucial for its effective use in laboratory and industrial settings, as it informs its formulation and potential applications.

Interesting facts

Interesting Facts about N-chloro-N-isopropyl-propan-2-amine

N-chloro-N-isopropyl-propan-2-amine, known within the scientific community for its intriguing attributes, is a compound that stands out due to several unique characteristics:

  • Functional Groups: This compound integrates the amine functional group with a chloro substituent, introducing interesting reactivity patterns that chemists find useful in organic synthesis.
  • Synthesis and Applications: N-chloro-N-isopropyl-propan-2-amine is often utilized in synthetic organic chemistry as a reagent for the introduction of isopropyl groups in various nucleophilic substitution reactions.
  • Biological Significance: The study of compounds like this one can provide insights into pharmacological effects, particularly in relation to structural activity relationships in drug design.
  • Environmental Considerations: Understanding the fate and transport of aminated compounds in the environment is crucial, as their behavior can significantly affect ecological and human health.

Fun Fact:

As noted by chemists, "the presence of chlorine can significantly influence the polarity and reactivity of amines, enhancing their utility in pharmaceutical applications." This highlights the importance of such compounds in the development of medications and other chemical products.

In summary, N-chloro-N-isopropyl-propan-2-amine represents a significant intersection of chemistry and biology, making it a valuable topic of study for both students and established scientists alike. Its versatile nature lends itself to further exploration in various fields of research.

Synonyms
N-chlorodiisopropylamine
24948-81-0
2-Propanamine, N-chloro-N-(1-methylethyl)-
EINECS 246-543-9
N-Chloro-N,N-diisopropylamine
N-chloro-N-propan-2-ylpropan-2-amine
CHLORODIISOPROPYLAMINE
S8LU935UVL
DTXSID2067036
N-CHLORO-N-(1-METHYLETHYL)-2-PROPANAMINE
RefChem:829491
DTXCID2037180
246-543-9
N-chloro-diisopropylamine
UNII-S8LU935UVL
N-chloro N,N-diisopropylamine
SCHEMBL6902960
SCHEMBL8213392
NS00027774