Skip to main content

2-bromoethyl N-(1-naphthyl)carbamate

ADVERTISEMENT
Identification
Molecular formula
C13H12BrNO2
CAS number
6316-10-1
IUPAC name
2-bromoethyl N-(1-naphthyl)carbamate
State
State

At room temperature, 2-bromoethyl N-(1-naphthyl)carbamate is typically a solid. It is generally stable when stored properly away from moisture and direct light.

Melting point (Celsius)
91.00
Melting point (Kelvin)
364.20
Boiling point (Celsius)
421.10
Boiling point (Kelvin)
694.30
General information
Molecular weight
293.15g/mol
Molar mass
293.1450g/mol
Density
1.4100g/cm3
Appearence

2-bromoethyl N-(1-naphthyl)carbamate typically appears as a white or off-white crystalline solid. The compound is generally odorless or may have a faint characteristic smell depending on the purity and storage conditions.

Comment on solubility

Solubility of 2-bromoethyl N-(1-naphthyl)carbamate

The solubility of 2-bromoethyl N-(1-naphthyl)carbamate can be influenced by its unique structural components. Understanding its solubility characteristics is essential for various applications. Here are some significant points to consider:

  • Polarity: Due to the presence of the polar carbamate functional group, this compound exhibits moderate polarity which affects its interactions with solvents.
  • Solvent Compatibility: 2-bromoethyl N-(1-naphthyl)carbamate is likely to be soluble in organic solvents such as:
    • Dichloromethane
    • Acetone
    • Ethyl acetate
  • Water Solubility: It is expected to have low solubility in water due to the hydrophobic characteristics of the naphthyl group, limiting its interaction with water molecules.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, leading to more favorable dissolution dynamics under elevated conditions.

In summary, while 2-bromoethyl N-(1-naphthyl)carbamate demonstrates moderate solubility in organic solvents, its low aqueous solubility is notable. Understanding these solubility characteristics is critical for its effective use in chemical reactions and formulations.

Interesting facts

Interesting Facts About 2-Bromoethyl N-(1-naphthyl)carbamate

2-Bromoethyl N-(1-naphthyl)carbamate, an intriguing compound, is significant due to its applications in medicinal chemistry and industrial synthesis. Here are some fascinating insights regarding this compound:

  • Versatile Derivative: This compound is a derivative of carbamate and is often used to modify the behavior of other molecules by acting as a reactive intermediate in chemical reactions.
  • Biological Activity: Research suggests that its structure may exhibit bioactivity, potentially offering applications in pharmacology, particularly as a precursor in drug development.
  • Role in Polymer Chemistry: 2-Bromoethyl N-(1-naphthyl)carbamate can be employed in the synthesis of various polymers, expanding its utility in material science.
  • Safety Considerations: As with many bromo compounds, handling requires precaution due to the potential for toxicity and environmental impact.
  • Research Potential: This compound continues to be a topic of interest, with ongoing studies focused on its reactivity and the mechanisms by which it influences biological systems.

In conclusion, the study of 2-bromoethyl N-(1-naphthyl)carbamate offers a rich field for exploration, enriching our understanding of chemistry's practical applications in both medicine and materials science.

Synonyms
25216-26-6
CARBAMIC ACID, (1-NAPHTHYL)-, 2-(BROMOETHYL) ESTER
KS9DD6EUF4
NSC 106894
(1-Naphthyl)carbamic acid 2-(bromoethyl) ester
BRN 3310950
1-Naphthylcarbamic acid, ester with 2-bromoethanol
NSC-106894
DTXSID30179874
4-12-00-03031 (Beilstein Handbook Reference)
RefChem:123375
DTXCID90102365
2-Bromoethyl naphthalen-1-ylcarbamate
2-BROMOETHYL N-(NAPHTHALEN-1-YL)CARBAMATE
UNII-KS9DD6EUF4
NSC106894
2-bromoethyl n-(1-naphthyl)carbamate
AKOS024330517