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Dinitrosecbutylphenylcarbamate

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Identification
Molecular formula
C11H13N3O5
CAS number
1721-26-2
IUPAC name
(2-tert-butyl-4,6-dinitro-phenyl) carbamate
State
State

At room temperature, Dinitrosecbutylphenylcarbamate is a solid. It is typically handled and stored in its solid form for industrial purposes, ensuring that it remains dry to prevent any premature reaction or degradation.

Melting point (Celsius)
96.00
Melting point (Kelvin)
369.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
297.27g/mol
Molar mass
297.2730g/mol
Density
1.4974g/cm3
Appearence

Dinitrosecbutylphenylcarbamate appears as a yellow crystalline solid. It is often supplied as finely ground powder or granules designed for particular applications. Its crystalline structure can reflect light, giving it a distinctive hue that is characteristic of many nitroaromatic compounds.

Comment on solubility

Solubility of (2-tert-butyl-4,6-dinitro-phenyl) carbamate

The solubility of (2-tert-butyl-4,6-dinitro-phenyl) carbamate, with the chemical formula C11H13N3O5, can be quite interesting due to its structural characteristics. Examine the following factors influencing its solubility:

  • Polar and Nonpolar Regions: This compound contains both polar (nitro and carbamate groups) and nonpolar (tert-butyl group) regions. The presence of polar functional groups generally increases solubility in polar solvents like water.
  • Hydrogen Bonding: The carbamate moiety is capable of forming hydrogen bonds. This enhances solubility in solvents that can engage in hydrogen bonding.
  • Solvent Interaction: While it is likely to be more soluble in organic solvents like methanol or ethanol, it may exhibit limited solubility in highly nonpolar solvents like hexane due to the steric hindrance from the tert-butyl group.

Overall, the solubility of (2-tert-butyl-4,6-dinitro-phenyl) carbamate can be summarized as:

  1. Relatively soluble in polar solvents.
  2. Limited solubility in nonpolar solvents.
  3. Enhanced solubility due to hydrogen bonding interactions.

In conclusion, while the solubility of (2-tert-butyl-4,6-dinitro-phenyl) carbamate can be expected to be favorable in certain solvents, it is important to consider the solvent environment and molecular interactions that influence its behavior in solution.

Interesting facts

Interesting Facts about (2-tert-butyl-4,6-dinitro-phenyl) carbamate

(2-tert-butyl-4,6-dinitro-phenyl) carbamate is a fascinating compound that belongs to the class of carbamates, which are organic derivatives of carbamic acid. This compound has garnered attention for several intriguing reasons:

  • Structural Complexity: The presence of a tert-butyl group and two nitro groups in its structure highlights the interesting relationship between sterics and electronic effects in chemical reactivity.
  • Biological Activity: Many derivatives of carbamates have been investigated for their potential biological activities, including insecticidal properties. This particular compound has sparked interest in the field of agrochemicals.
  • Application in Research: Compounds like (2-tert-butyl-4,6-dinitro-phenyl) carbamate are often used as intermediates in the synthesis of more complex organic molecules, making them valuable in medicinal chemistry and materials science.

This compound exemplifies how the modification of simple functional groups can lead to significant changes in a molecule's properties and applications. In the world of chemistry, it is often said that “the devil is in the details”, and this phrase rings true when examining the structure and applications of well-designed compounds like this one.

As research continues to evolve, one can only imagine the new discoveries and innovations that might arise from compounds with such intriguing molecular designs.

Synonyms
13268-96-7
2-tert-Butyl-4,6-dinitrophenol carbamate
UC 21427
2-tert-Butyl-4,6-dinitrophenyl carbamate
CARBAMIC ACID, 2-tert-BUTYL-4,6-DINITROPHENYL ESTER
DTXSID20927765
2-t-butyl-4,6-dinitrophenyl carbamate
2-tert-Butyl-4,6-dinitrophenyl hydrogen carbonimidate
Phenol, 2-(1,1-dimethylethyl)-4,6-dinitro-, carbamate (ester)