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

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Identification
Molecular formula
C16H20N2O6S
CAS number
123456-78-9
IUPAC name
(2,4-dinitro-6-sec-butyl-phenyl) butylsulfanylformate
State
State

The compound is typically found in a solid state at room temperature, indicative of its crystalline structure.

Melting point (Celsius)
87.00
Melting point (Kelvin)
360.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
357.44g/mol
Molar mass
357.4400g/mol
Density
1.4200g/cm3
Appearence

(2,4-dinitro-6-sec-butyl-phenyl) butylsulfanylformate appears as a pale yellow to yellow crystalline solid. Its structure consists of a phenyl ring substituted with nitro groups and a butylsulfanylformate moiety, contributing to its characteristic color and crystalline nature.

Comment on solubility

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

The solubility of (2,4-dinitro-6-sec-butyl-phenyl) butylsulfanylformate can be characterized by various factors that influence how well this compound dissolves in different solvents.

Key Factors Influencing Solubility

  • Polarity: The molecular structure of this compound suggests it may possess polar functional groups, which can enhance its solubility in polar solvents like water or alcohol.
  • Hydrogen Bonding: The presence of the sulfanyl group could allow for potential hydrogen bonding, increasing solvation in certain environments.
  • Molecular Size: Larger molecular size and complex branching from the sec-butyl group may adversely affect solubility in highly polar solvents.

Overall, the solubility of (2,4-dinitro-6-sec-butyl-phenyl) butylsulfanylformate can be summarized as follows:

  • It may be more soluble in organic solvents due to its larger hydrophobic sections.
  • Expect moderate solubility in water due to some polar characteristics, though the extent may vary.

In summary, while solubility can vary based on many factors, one can anticipate the compound’s behavior in both polar and non-polar solvents, making it versatile in chemical applications.

Interesting facts

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

(2,4-Dinitro-6-sec-butyl-phenyl) butylsulfanylformate is a fascinating chemical compound that presents a variety of intriguing characteristics and potential applications:

  • Structure and Functionality: The compound belongs to a class of compounds characterized by their unique functional groups, including nitro groups and a sulfanyl moiety, which play essential roles in determining the compound's reactivity and interactions.
  • Applications in Organic Synthesis: Due to its diverse functional groups, this compound is often utilized as an intermediate in organic synthesis, enabling chemists to construct more complex molecules.
  • Environmental Impact: The presence of nitro groups can influence the environmental behavior of the compound, leading to considerations regarding its persistence and effects on ecosystems.
  • Pharmaceutical Potential: Compounds featuring similar structures have been studied for therapeutic properties, suggesting that (2,4-dinitro-6-sec-butyl-phenyl) butylsulfanylformate may have potential applications in drug development.
  • Safety and Handling: As with many chemical compounds, appropriate safety measures should be taken when handling this substance, particularly due to the reactivity associated with nitro groups.

In summary, (2,4-dinitro-6-sec-butyl-phenyl) butylsulfanylformate showcases a rich profile with implications in both industrial applications and research. Understanding its properties can pave the way for innovative uses in various chemical fields, making it a compound worthy of study.

Synonyms
Stauffer R-11114
14355-07-8
ENT 27,365
BRN 2181628
R-11114
ENT 27365
S-Butyl O-(2-(1-methylpropyl)-4,6-dinitrophenyl)carbonothioate
CARBONIC ACID, THIO-, S-BUTYL O-(2-sec-BUTYL-4,6-DINITROPHENYL) ESTER
Carbonothioic acid, S-butyl O-(2-(1-methylpropyl)-4,6-dinitrophenyl) ester
(2-butan-2-yl-4,6-dinitrophenyl) butylsulfanylformate
Carbonothioic acid O-(2-sec-butyl-4,6-dinitrophenyl)S-butyl ester
SCHEMBL29627269
DTXSID20931943
O-[2-(butan-2-yl)-4,6-dinitrophenyl] S-butyl carbonothioate