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2-chloroethyl N-(1-naphthyl)carbamate

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Identification
Molecular formula
C13H12ClNO2
CAS number
3772-05-4
IUPAC name
2-chloroethyl N-(1-naphthyl)carbamate
State
State

At room temperature, 2-chloroethyl N-(1-naphthyl)carbamate is found in a solid state, typically as a crystalline or powdery substance. This solid form is due to the molecular structure and intermolecular forces present in the compound.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
263.70g/mol
Molar mass
263.7280g/mol
Density
1.3050g/cm3
Appearence

2-Chloroethyl N-(1-naphthyl)carbamate is typically a crystalline solid. The compound is often observed as a white or off-white powder, sometimes formed as crystals. Its appearance is consistent with many carbamate-based compounds, which often take solid forms at room temperature.

Comment on solubility

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

The solubility of 2-chloroethyl N-(1-naphthyl)carbamate in various solvents can provide insight into its chemical behavior and potential applications. Understanding its solubility characteristics is crucial for researchers and industrial applications. Here are some key points regarding its solubility:

  • Polar Solvents: Due to the presence of the carbamate functional group, which has polar characteristics, 2-chloroethyl N-(1-naphthyl)carbamate is expected to have moderate solubility in polar solvents such as water and methanol.
  • Non-Polar Solvents: The naphthalene moiety suggests that the compound may exhibit better solubility in non-polar solvents like hexane or toluene, owing to its hydrophobic properties.
  • Temperature Dependence: Like many organic compounds, its solubility may vary with temperature, typically increasing as the temperature rises.
  • pH Influence: The solubility can also be affected by pH, particularly because carbamate groups can be protonated under acidic conditions, altering its solubility profile.

In summary, the solubility of 2-chloroethyl N-(1-naphthyl)carbamate is influenced by both its structural components and the choice of solvent. Careful consideration of these factors is essential for applications that involve this compound, such as in pharmaceuticals or agrochemicals.

Interesting facts

Interesting Facts about 2-Chloroethyl N-(1-naphthyl)carbamate

2-Chloroethyl N-(1-naphthyl)carbamate is a fascinating chemical compound that has piqued the interest of scientists for its potential applications and unique properties. Below are some engaging facts about this compound:

  • Pharmaceutical Relevance: This compound belongs to the class of carbamates, which are known for their applications in medicinal chemistry. They often exhibit biological activity that can lead to the development of new pharmaceuticals.
  • Structural Features: The presence of the naphthyl group in its structure contributes to the compound’s intriguing electronic properties, enhancing its reactivity and potential for interaction with biological systems.
  • Synthesis: The synthesis of 2-chloroethyl N-(1-naphthyl)carbamate typically involves well-established organic reactions. Understanding these synthetic pathways is essential for chemists aiming to work with or create derivatives of this compound.
  • Biological Activity: Like many carbamates, this compound may exhibit insecticidal or herbicidal properties, making it relevant in the field of agricultural chemistry as well as environmental science.
  • Safety Considerations: Due to its potentially toxic nature, handling of 2-chloroethyl N-(1-naphthyl)carbamate necessitates proper safety protocols in laboratory settings to mitigate any health risks associated with exposure.
  • Research Significance: Continued research into this compound may lead to new insights in organic synthesis and the development of chemical agents that could be beneficial in various industrial applications.

Overall, 2-chloroethyl N-(1-naphthyl)carbamate represents a compound with both historical significance and contemporary relevance, showcasing the intricate connections between basic chemical research and practical applications in industry and healthcare.

Synonyms
2-CHLOROETHYL N-(1-NAPHTHYL)CARBAMATE
RefChem:470427
667-341-0
25216-25-5
1-NAPHTHALENECARBAMIC ACID, 2-CHLOROETHYL ESTER
2-chloroethyl naphthalen-1-ylcarbamate
2-CHLOROETHYL N-(NAPHTHALEN-1-YL)CARBAMATE
CB 14
NSC 106881
BRN 3310939
Carbamic acid, 1-naphthalenyl-, 2-chloroethyl ester
DTXSID70179873
NSC106881
AKOS024335274
NSC-106881