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(4-amino-3,5-dichlorophenyl)thiocyanate

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Identification
Molecular formula
C7H4Cl2N2S
CAS number
3289-06-9
IUPAC name
(4-amino-3,5-dichloro-phenyl) thiocyanate
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
141.00
Melting point (Kelvin)
414.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
219.10g/mol
Molar mass
219.1050g/mol
Density
1.5560g/cm3
Appearence

(4-amino-3,5-dichlorophenyl)thiocyanate typically appears as a crystalline solid. The exact color can vary slightly depending on purity, but it often appears white to off-white.

Comment on solubility

Solubility of (4-amino-3,5-dichloro-phenyl) thiocyanate

The solubility of (4-amino-3,5-dichloro-phenyl) thiocyanate can be influenced by several factors, including temperature, pH, and the presence of other ions or compounds in solution.

General Solubility Characteristics:

  • Water solubility: This compound is typically sparingly soluble in water. The presence of the amino group may contribute some degree of solubility due to its capacity for hydrogen bonding, yet the bulkiness and halogen substituents reduce overall solubility.
  • Solubility in organic solvents: Often, (4-amino-3,5-dichloro-phenyl) thiocyanate exhibits better solubility in organic solvents such as ethanol or acetone. This makes it more accessible for reactions in organic chemistry contexts.

When assessing solubility, remember that “like dissolves like.” Thus, polar solvents will be more effective for dissolving compounds with polar functional groups, such as the amino group present in this thiocyanate. Additionally, variations in temperature can play a significant role; increasing the temperature of a solvent often enhances the solubility of solid compounds:

  1. Increased kinetic energy: Higher temperatures can increase molecular movement and interaction, facilitating dissolution.
  2. Changes in solvation dynamics: At elevated temperatures, the solvation of molecules may also be more efficient, leading to greater solubility.

Finally, understanding the nuances of the solubility of (4-amino-3,5-dichloro-phenyl) thiocyanate not only lends insight into its chemical behavior but also aids in predicting its applications in various fields of chemistry.

Interesting facts

Understanding (4-amino-3,5-dichloro-phenyl) thiocyanate

(4-amino-3,5-dichloro-phenyl) thiocyanate is a fascinating compound that holds significance in various spheres of chemistry and industry. This compound is known for its unique structural features and functional versatility.

Key Characteristics

  • Substituted Aromatic Compound: The presence of amino and chloro groups on the phenyl ring contributes to its reactivity, making it an interesting subject for organic synthesis and modification.
  • Thiocyanate Functional Group: The thiocyanate group (–SCN) is known for its ability to form coordination complexes, which is vital in fields such as bioinorganic chemistry and environmental chemistry.
  • Applications: This compound is often explored in pesticide formulations, where its unique chemical properties may enhance efficacy against pests.

Chemical Behavior

The reactivity of (4-amino-3,5-dichloro-phenyl) thiocyanate can be attributed to the electron-withdrawing effects of chlorine atoms, which can influence nucleophilic and electrophilic interactions. Such interactions provide opportunities for:

  • **Formation of derivatives:** This compound can be transformed into various derivatives, broadening its application potential.
  • **Biochemical studies:** It serves as a potent tool in biochemical research due to the ability of thiocyanate ions to mimic certain biologically relevant interactions.

Future Research

There is ongoing research into the potential usages of this compound in various fields, including but not limited to:

  • Pharmaceuticals: Investigating its role in drug design and synthesis could unveil new therapeutic pathways.
  • Environmental Science: Its interactions with biological systems make it a candidate for studying environmental impacts and contaminant behavior.

In conclusion, (4-amino-3,5-dichloro-phenyl) thiocyanate is not only a compound of interest due to its unique structural properties but also because of its extensive possibilities for future applications and research. As scientists continue to explore its characteristics, we could see innovative solutions arising from this compound.

Synonyms
2,6-Dichloro-4-thiocyanatoaniline
14030-85-4
ANILINE, 2,6-DICHLORO-4-THIOCYANATO-
BRN 2806377
DTXSID40161306
DTXCID6083797
4-Amino-3,5-dichlorophenyl thiocyanate
(4-amino-3,5-dichlorophenyl) thiocyanate
SCHEMBL10414212