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(4-nitrophenyl) N-ethylcarbamate

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Identification
Molecular formula
C9H10N2O4
CAS number
59263-96-2
IUPAC name
(4-nitrophenyl) N-ethylcarbamate
State
State

At room temperature, (4-nitrophenyl) N-ethylcarbamate is typically a solid, particularly in crystalline form.

Melting point (Celsius)
83.00
Melting point (Kelvin)
356.15
Boiling point (Celsius)
355.20
Boiling point (Kelvin)
628.30
General information
Molecular weight
210.19g/mol
Molar mass
0.0000g/mol
Density
1.3250g/cm3
Appearence

(4-nitrophenyl) N-ethylcarbamate appears as a solid, often in the form of crystalline powder, usually pale yellow. This is due to the presence of the nitro group which commonly imparts a yellowish hue to organic compounds.

Comment on solubility

Solubility of (4-nitrophenyl) N-ethylcarbamate

(4-nitrophenyl) N-ethylcarbamate is a compound with interesting solubility characteristics that can influence its applications in various fields. Understanding its solubility can help in areas such as formulation and synthesis.

General Solubility Characteristics:

The solubility of (4-nitrophenyl) N-ethylcarbamate can be examined in multiple solvents, and it is generally affected by the following factors:

  • Polarity of Solvents: This compound is more likely to dissolve in polar organic solvents compared to non-polar solvents due to its functional groups.
  • Temperature Influence: As with many organic compounds, increasing temperature may enhance its solubility in a given solvent.
  • Hydrogen Bonding: The presence of electron-withdrawing groups such as the nitro group may affect the ability of the compound to engage in hydrogen bonding with solvents.

Solubility Insights:

While specific solubility data may vary, compounds like (4-nitrophenyl) N-ethylcarbamate often exhibit the following:

  • Moderate solubility in ethanol and other polar aprotic solvents.
  • Limited solubility in water, primarily due to hydrophobic alkyl groups.

In summary, the solubility of (4-nitrophenyl) N-ethylcarbamate is primarily influenced by its structural characteristics and the properties of the solvent used. A comprehensive understanding of these factors is crucial for its effective use in chemical processes.

Interesting facts

Interesting Facts About (4-nitrophenyl) N-ethylcarbamate

(4-nitrophenyl) N-ethylcarbamate is a fascinating organic compound that falls under the category of carbamates. This class of compounds is known for its diverse applications, particularly in the fields of agriculture and pharmaceuticals. Here are some intriguing aspects of this particular compound:

  • Derived Features: The presence of a nitro group on the phenyl ring significantly influences the compound's properties. Nitro groups can enhance electron-withdrawing abilities, which can alter the reactivity and biological activity of the molecule.
  • Biological Activity: Carbamates are often evaluated for their potential as pesticides or herbicides. The interaction of (4-nitrophenyl) N-ethylcarbamate with various biological systems can yield important insights into its safety and efficacy in agricultural applications.
  • Mechanism of Action: Many carbamates function by inhibiting acetylcholinesterase, an enzyme critical for neurotransmission in both plants and animals. Studying (4-nitrophenyl) N-ethylcarbamate may reveal mechanisms that can be exploited for pest control strategies.
  • Research Applications: This compound can serve as a crucial intermediate in the synthesis of other chemicals, allowing chemists to explore novel organic transformations or develop new materials with tailored properties.

The study of (4-nitrophenyl) N-ethylcarbamate not only enhances our understanding of organic chemistry but also connects the dots to real-world applications that affect agriculture and pharmacology. As researchers continue to investigate its potential, one can only anticipate the exciting advancements that may arise from this compound!

Synonyms
4-Nitrophenyl ethylcarbamate
17576-41-9
(4-nitrophenyl) N-ethylcarbamate
Ethylcarbamic Acid 4-Nitrophenyl Ester
CARBAMIC ACID, ETHYL-, 4-NITROPHENYL ESTER
CARBAMICACID,ETHYL-,4-NITROPHENYLESTER
MFCD01738228
Ethylcarbamic Acid 4-Nitrophenyl Ester (~90%)
4-NITROPHENYL N-ETHYLCARBAMATE
BRN 1975958
AI3-27285
4-Nitrophenylethylcarbamate
SCHEMBL1695035
SCHEMBL3398600
CHEMBL2288439
DTXSID40170019
SAA57641
Ethylcarbamic Acid p-Nitrophenyl Ester
DB-319593
CS-0094883
D75660