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Dinoseb

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Identification
Molecular formula
C14H14N2O5
CAS number
88-85-7
IUPAC name
[2-(1-methylheptyl)-4,6-dinitro-phenyl] but-2-enoate
State
State

Dinoseb exists as a solid at room temperature.

Melting point (Celsius)
38.00
Melting point (Kelvin)
311.15
Boiling point (Celsius)
356.00
Boiling point (Kelvin)
629.15
General information
Molecular weight
312.28g/mol
Molar mass
312.3120g/mol
Density
1.2820g/cm3
Appearence

Dinoseb is a yellow, crystalline solid. It has a distinct appearance often characterized by its bright yellow hue, which can aid in its identification. The crystals are typically small and can be powdery.

Comment on solubility

Solubility of [2-(1-methylheptyl)-4,6-dinitro-phenyl] but-2-enoate

The solubility of the compound [2-(1-methylheptyl)-4,6-dinitro-phenyl] but-2-enoate is characterized by its unique structure, impacting its interaction with various solvents. Generally, the solubility of organic compounds can be influenced by the following factors:

  • Polarity: Due to the presence of both alkyl and nitro groups, this compound exhibits a mixed polarity.
  • Hydrogen Bonding: The ability to form hydrogen bonds can greatly enhance solubility in polar solvents.
  • Hydrophobic Effect: The long alkyl chain contributes to hydrophobic interactions, making it less soluble in water but more soluble in organic solvents like ethanol, acetone, or hexane.

In practical terms, it is likely to dissolve poorly in aqueous environments but might find better solubility in organic phases. This can be summarized by the phrase, "Likes dissolve likes," indicating that non-polar solvents would facilitate better solubility for this compound.

To conclude, understanding the solubility behavior of [2-(1-methylheptyl)-4,6-dinitro-phenyl] but-2-enoate is essential for predicting its behavior in various chemical applications and interactions.

Interesting facts

Interesting Facts about [2-(1-methylheptyl)-4,6-dinitro-phenyl] but-2-enoate

[2-(1-methylheptyl)-4,6-dinitro-phenyl] but-2-enoate is a fascinating compound that showcases the intricate relationships between molecular structure and chemical behavior. As a derivative of but-2-enoic acid, this compound contains a unique arrangement of functional groups that contribute to its distinct properties.

Key Features of the Compound:

  • Structural Diversity: The presence of both dinitro and butenoate functional groups in its structure helps explain many of its chemical reactions.
  • Biosignificant Potential: Compounds like this can serve as intermediates in organic synthesis, potentially leading to the creation of pharmaceuticals or agrochemicals.
  • Stability and Reactivity: The dinitro substitutions may affect the compound's stability and reactivity, making it a subject of interest for further studies in reactivity patterns.

Quote: "Understanding the architecture of organic compounds paves the way for innovative applications in medicine and materials science."

This compound is an excellent example of how modifications in the molecular framework can lead to variations in chemical behavior. Chemists and researchers often explore such compounds to uncover new pathways for synthesis or to optimize existing reactions. Its unique arrangement also makes it a candidate for exploration in fields ranging from environmental science to pharmacology. The ongoing study of compounds like [2-(1-methylheptyl)-4,6-dinitro-phenyl] but-2-enoate continues to unveil the complexity of chemical interactions and their implications in real-world applications.

Synonyms
(2,4-dinitro-6-octan-2-ylphenyl) but-2-enoate
6119-92-2
2,4-DNOPC
2-(1-Methylheptyl)-4,6-dinitrophenyl crotonate
(E)-2,4-Dinitro-6-(octan-2-yl)phenyl but-2-enoate
2-Butenoic acid, 2-(1-methylheptyl)-4,6-dinitrophenyl ester
SCHEMBL676763
Dinitro(1-methylheptyl)phenyl crotonate, commercial grade (78%)
DTXSID7021732
NIOPZPCMRQGZCE-UHFFFAOYSA-N
AKOS024319004
NS00098681
2,4-dinitro-6-(octan-2-yl)phenyl but-2-enoate