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Pentyl 2-thiocyanatoacetate

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Identification
Molecular formula
C9H15NO2S
CAS number
NULL
IUPAC name
pentyl 2-thiocyanatoacetate
State
State

At room temperature, pentyl 2-thiocyanatoacetate is a liquid. It has low volatility and should be stored in a sealed container to avoid exposure to moisture and air which may cause decomposition over time.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
258.00
Boiling point (Kelvin)
531.15
General information
Molecular weight
203.30g/mol
Molar mass
203.2960g/mol
Density
1.0308g/cm3
Appearence

Pentyl 2-thiocyanatoacetate is typically a colorless to pale yellow liquid. It is relatively stable under normal conditions, but proper handling is advised as with many thiocyanato compounds.

Comment on solubility

Solubility of Pentyl 2-thiocyanatoacetate

Pentyl 2-thiocyanatoacetate, a chemical compound with the formula C6H10N2OS, exhibits interesting solubility characteristics. In the context of its solubility, one can make several observations:

  • Polar Nature: The presence of the thiocyanate group contributes to the polar nature of the compound, which can enhance its solubility in polar solvents.
  • Solvent Compatibility: Pentyl 2-thiocyanatoacetate is expected to be soluble in common organic solvents such as ethanol and acetone, while showing lesser solubility in non-polar solvents.
  • Temperature Effects: Generally, an increase in temperature can lead to higher solubility, particularly in organic solvents.
  • Application Relevance: The solubility properties are crucial in its applications, especially in synthesis and formulation in chemical industries.

In summary, the solubility of pentyl 2-thiocyanatoacetate is largely influenced by its molecular structure and the nature of the solvent. Understanding these solubility dynamics is essential for effectively utilizing this compound in various chemical processes.

Interesting facts

Interesting Facts About Pentyl 2-Thiocyanatoacetate

Pentyl 2-thiocyanatoacetate is a fascinating compound that belongs to the diverse family of thiocyanates. Here are some captivating aspects that highlight its significance in the field of chemistry:

  • Biological Relevance: Pentyl 2-thiocyanatoacetate is studied for its potential biological activity. Thiocyanate derivatives have been associated with various physiological effects, making them of interest in drug design and pharmacology.
  • Versatile Functional Group: The thiocyanate group (-SCN) is known for its ability to participate in nucleophilic substitution reactions, which makes pentyl 2-thiocyanatoacetate a valuable intermediate in synthesis. It can act as a building block for creating more complex molecules.
  • Use in Material Science: Compounds like pentyl 2-thiocyanatoacetate have potential applications in the development of advanced materials. Their unique chemical properties can be harnessed to create polymers or coatings with enhanced characteristics.
  • Environmental Chemistry: The study of thiocyanates is crucial in understanding their environmental impact, especially in agricultural runoff where they can influence soil and water chemistry.

As a chemistry student or a researcher exploring the realm of organic compounds, pentyl 2-thiocyanatoacetate exemplifies the intricate connections between structure and function in chemical compounds. It serves as a reminder that even specialized substances can hold the key to significant scientific advancements.

Synonyms
Thiocyanatoacetic acid pentyl ester
5439-31-6
ACETIC ACID, THIOCYANATO-, PENTYL ESTER
Thiocyano-essigsaeure-N-amyl-ester
Pentyl thiocyanatoacetate
JFO57AKU2O
NSC-15095
NSC 15095
Thiocyano-essigsaeure-N-amyl-ester [German]
UNII-JFO57AKU2O
WLN: NCS1VO5
DTXSID40202763
NSC15095
ACETIC ACID, 2-THIOCYANATO-, PENTYL ESTER