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Diethylcarbamazine

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Identification
Molecular formula
C10H21N2O
CAS number
90-89-1
IUPAC name
2-(diethylamino)ethyl N-phenylcarbamate
State
State
Diethylcarbamazine is typically a solid at room temperature, appearing as a crystalline powder.
Melting point (Celsius)
47.50
Melting point (Kelvin)
320.65
Boiling point (Celsius)
318.50
Boiling point (Kelvin)
591.65
General information
Molecular weight
240.34g/mol
Molar mass
240.3350g/mol
Density
1.0064g/cm3
Appearence

Diethylcarbamazine appears as a white to slightly off-white crystalline powder. It is usually odorless and soluble in many organic solvents such as ethanol and chloroform, but it is practically insoluble in water.

Comment on solubility

Solubility of 2-(diethylamino)ethyl N-phenylcarbamate

The solubility of 2-(diethylamino)ethyl N-phenylcarbamate is influenced by several factors, making it an interesting compound to study. Here are some key points regarding its solubility:

  • Polarity: The presence of both diethylamino and phenylcarbamate groups contributes to a polar nature, which generally enhances solubility in polar solvents.
  • Solvent Compatibility: This compound is likely to be soluble in polar organic solvents such as:
    • Dimethyl sulfoxide (DMSO)
    • Acetonitrile
    • Alcohols
  • Limited Aqueous Solubility: Due to its organic structure, 2-(diethylamino)ethyl N-phenylcarbamate is expected to have limited solubility in water, a common trend for many organic compounds.
  • Temperature Effects: The solubility may also vary with temperature, as higher temperatures typically increase solubility for most solids in liquids.

Understanding the solubility of 2-(diethylamino)ethyl N-phenylcarbamate is crucial for its applications in various industries, particularly in pharmacology where solubility can affect bioavailability and therapeutic efficacy.

Interesting facts

Interesting Facts about 2-(diethylamino)ethyl N-phenylcarbamate

The compound known as 2-(diethylamino)ethyl N-phenylcarbamate is a fascinating chemical with a variety of applications and implications in different fields.

Key Highlights

  • Biological Activity: This compound exhibits interesting biological activity, making it a topic of interest in medicinal chemistry and pharmacology.
  • Mechanism of Action: Its structure allows it to interact with biological systems in specific ways, potentially influencing enzyme activities or neurotransmitter pathways.
  • Use in Research: Researchers often utilize this compound in studies related to drug development, particularly in exploring mechanisms of action for neurological disorders.
  • Safety and Toxicology: Like many nitrogen-containing compounds, understanding the safety profile and potential toxicity is crucial for applications in pharmaceuticals.

As noted by many scientists in the field, “The key to advancing pharmacological studies lies in gaining a deeper understanding of compounds like 2-(diethylamino)ethyl N-phenylcarbamate.” This statement emphasizes the importance of such compounds in the continual search for new therapeutics.

Applications

  • As an intermediate in synthesizing novel pharmaceutical agents.
  • In the study of enzyme inhibition, especially in choline acetyltransferase research.
  • Potential role in the development of pesticides due to its carbamate structure.

In summary, the exploration of 2-(diethylamino)ethyl N-phenylcarbamate helps unravel new biochemical pathways and fosters innovation in pharmaceutical sciences. Its intriguing properties make it a compound worth studying for anyone keen on the intersections of chemistry and biology.

Synonyms
2-(diethylamino)ethyl N-phenylcarbamate
Carbamic acid, phenyl-, 2-(diethylamino)ethyl ester
666-953-5
Ethanol, 2-diethylamino-, carbanilate
3898-59-7
2-Diethylaminoethanol carbanilate
Carbanilic acid, 2-diethylaminoethyl ester
BRN 2807628
4-12-00-00729 (Beilstein Handbook Reference)
SCHEMBL9324886
DTXSID30192265
AKOS024334933