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(2,4-dinitro-6-sec-butyl-phenyl) ethylsulfanylformate

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Identification
Molecular formula
C12H14N2O6S
CAS number
.null
IUPAC name
(2,4-dinitro-6-sec-butyl-phenyl) ethylsulfanylformate
State
State

This compound exists as a crystalline solid at room temperature. It is stable under normal conditions but should be handled with care due to the presence of nitro groups, which can sometimes make compounds more sensitive.

Melting point (Celsius)
78.00
Melting point (Kelvin)
351.15
Boiling point (Celsius)
289.00
Boiling point (Kelvin)
562.15
General information
Molecular weight
357.39g/mol
Molar mass
357.3940g/mol
Density
1.3600g/cm3
Appearence

This compound is typically a yellowish to orange crystalline solid, which is consistent with many dinitro-substituted aromatic compounds. The presence of nitro groups usually imparts a strong color to the compound.

Comment on solubility

Solubility of (2,4-dinitro-6-sec-butyl-phenyl) ethylsulfanylformate

The solubility of (2,4-dinitro-6-sec-butyl-phenyl) ethylsulfanylformate is a fascinating topic of study due to its complex structure. Understanding how this compound behaves in various solvents can provide insights into its chemical interactions and potential applications.

Factors Influencing Solubility

The solubility of this compound can be influenced by several factors, including:

  • Polarity: The presence of both polar and nonpolar groups in the structure affects solubility in polar and nonpolar solvents.
  • Hydrogen bonding: Compounds capable of hydrogen bonding typically have higher solubility in polar solvents like water.
  • Temperature: In many cases, solubility increases with temperature, allowing more of the compound to dissolve.
  • Presence of co-solvents: Mixing different solvents can enhance overall solubility due to varying solvation dynamics.

Common Solvents

In the case of (2,4-dinitro-6-sec-butyl-phenyl) ethylsulfanylformate, the following solvents might be considered:

  • Acetone: A medium that may dissolve the compound due to its ability to interact with both polar and nonpolar regions.
  • Dichloromethane: Often effective for dissolving organic compounds similar in nature.
  • Water: While less likely due to nonpolar characteristics, certain conditions might allow for limited solubility.

As a conclusion, the solubility of (2,4-dinitro-6-sec-butyl-phenyl) ethylsulfanylformate varies with solvent choice and environmental conditions, making it an intriguing compound for further exploration in solubility studies. Understanding its solubility behavior opens up discussions for its applications in different chemical processes and formulations.

Interesting facts

Interesting Facts about (2,4-Dinitro-6-sec-butyl-phenyl) Ethylsulfanylformate

(2,4-Dinitro-6-sec-butyl-phenyl) ethylsulfanylformate is a fascinating compound that embodies the intricate relationships between structure and function in organic chemistry. Here are some captivating insights:

  • Unique Functional Groups: This compound contains both nitro and thioester functional groups, which significantly influence its reactivity and potential applications.
  • Pesticidal Applications: Given the presence of the dinitro and sulfanyl groups, compounds like this have been investigated for their effectiveness in agriculture as potential pesticides or herbicides.
  • Synthetic Pathways: The synthesis of such compounds may involve various complex organic reactions, showcasing the creativity and innovation involved in modern synthetic chemistry.
  • Environmental Implications: As a chemical scientist, it's essential to consider the environmental impact of using compounds with nitro groups, as they can contribute to the generation of harmful environmental pollutants.
  • Research Potential: The combination of a bulky sec-butyl group with dinitro substitutions can result in interesting steric and electronic properties, making it a subject of interest for research in material science and medicinal chemistry.
  • Biological Significance: The compound's structure suggests potential activity against specific biological targets, which may inspire further studies on its pharmacological effects.

The exploration of (2,4-dinitro-6-sec-butyl-phenyl) ethylsulfanylformate highlights the vast realm of organic chemistry and underscores the importance of understanding the nuances of chemical compounds.

Synonyms
Stauffer R-11260
6074-15-3
ENT 27,367
NSC 190963
BRN 2176836
R-11260
S-Ethyl O-(2-(1-methylpropyl)-4,6-dinitrophenyl) carbonothioate
CARBONIC ACID, THIO-, O-(2-sec-BUTYL-4,6-DINITROPHENYL) S-ETHYL ESTER
Carbonothioic acid, S-ethyl O-(2-(1-methylpropyl)-4,6-dinitrophenyl) ester
O-(2-sek.Butyl-4,6-dinitrofenyl)-S-ethylester kyseliny thiouhlicite [Czech]
O-(2-sek.Butyl-4,6-dinitrofenyl)-S-ethylester kyseliny thiouhlicite
DTXSID20976213
(2-Butan-2-yl-4,6-dinitrophenyl)ethylsulfanylformate
O-[2-(Butan-2-yl)-4,6-dinitrophenyl] S-ethyl carbonothioate