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Edrophonium

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Identification
Molecular formula
C10H16ClNO2
CAS number
114-32-9
IUPAC name
ethyl N-[(dimethylamino)methyl]carbamate
State
State

At room temperature, Edrophonium is typically found as a solid.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.15
Boiling point (Celsius)
43.00
Boiling point (Kelvin)
316.15
General information
Molecular weight
203.27g/mol
Molar mass
203.2710g/mol
Density
1.1600g/cm3
Appearence

Ethyl N-[(dimethylamino)methyl]carbamate, commonly known as Edrophonium, is typically presented as a crystalline powder. It is colorless to slightly white in appearance.

Comment on solubility

Solubility of Ethyl N-[(dimethylamino)methyl]carbamate

Ethyl N-[(dimethylamino)methyl]carbamate, with its unique molecular structure, exhibits distinct solubility characteristics that make it noteworthy in various applications. Here’s what you need to know:

  • Polarity: The presence of both ethyl and dimethylamino groups contributes to the compound's overall polarity. This aspect influences its solubility in solvents.
  • Solvent Compatibility: Typically, compounds that are polar tend to dissolve well in polar solvents such as water and alcohols. Ethyl N-[(dimethylamino)methyl]carbamate is expected to have a higher solubility in organic polar solvents.
  • Temperature Dependency: Like many chemical compounds, the solubility of ethyl N-[(dimethylamino)methyl]carbamate may increase with temperature, allowing for higher concentrations in solution as the kinetic energy of the molecules rises.
  • Hydrogen Bonding: The presence of functional groups capable of hydrogen bonding, such as the amine and carbamate functionalities, may enhance its solubility in certain solvents, contributing to interactions that stabilize solvation.

In summary, the solubility of ethyl N-[(dimethylamino)methyl]carbamate is influenced by its polarity, functional groups, and solvent environment. Understanding these factors is crucial for optimizing its use in various chemical processes and applications.

Interesting facts

Interesting Facts about Ethyl N-[(dimethylamino)methyl]carbamate

Ethyl N-[(dimethylamino)methyl]carbamate is a fascinating compound with diverse applications and intriguing properties. Here are some key highlights:

  • Chemical Classification: This compound belongs to the class of carbamates, which are esters or salts of carbamic acid. Carbamates play a significant role in both biological and synthetic chemistry.
  • Biological Relevance: Many carbamate derivatives are known for their function as insecticides and herbicides. Ethyl N-[(dimethylamino)methyl]carbamate's structure hints at potential biological activity, making it a valuable subject of research for agrochemical applications.
  • Pharmaceutical Potential: Compounds featuring dimethylamino groups often engage in intriguing interactions within biological systems. The presence of this group may impart the compound with pharmacological properties, allowing chemists to explore its potential use in drug development.
  • Synthetic Versatility: The carbamate functional group is well-known for its versatility in synthetic organic chemistry. Ethyl N-[(dimethylamino)methyl]carbamate can serve as a useful intermediate for synthesizing more complex molecules.
  • Research Avenue: The modifications to the dimethylamino group and its location in the molecule present a myriad of opportunities for chemists to delve deeper into structure-activity relationships (SAR) within the compound class.

In conclusion, ethyl N-[(dimethylamino)methyl]carbamate is a compound that embodies the intersection of organic chemistry and biology. Its unique structure may hold the key to unlocking new innovations in pharmaceuticals and agricultural products, making it an exciting topic of study for both aspiring and seasoned chemists.

Synonyms
Ethyl dimethylaminomethylcarbamate
6781-05-1
BRN 1905026
CARBAMIC ACID, DIMETHYLAMINOMETHYL-, ETHYL ESTER
DTXSID70218059
DTXCID40140550
AKOS006348924