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Pentyl N-hydroxycarbamate

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Identification
Molecular formula
C6H13NO3
CAS number
54194-56-6
IUPAC name
pentyl N-hydroxycarbamate
State
State

At room temperature, it is generally observed as a liquid.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
277.00
Boiling point (Kelvin)
550.15
General information
Molecular weight
147.17g/mol
Molar mass
147.1720g/mol
Density
1.0998g/cm3
Appearence

Pentyl N-hydroxycarbamate typically appears as a colorless to light yellow liquid. It can sometimes present mild turbidity or opalescence.

Comment on solubility

Solubility of Pentyl N-hydroxycarbamate

Pentyl N-hydroxycarbamate, with the chemical formula C6H13NO3, exhibits interesting solubility characteristics that are worth noting:

  • Polar vs. Non-polar Solvents: This compound is likely to be soluble in polar solvents due to the presence of the hydroxy (-OH) functional group, which can form hydrogen bonds.
  • Water Solubility: The solubility in water can be expected to be moderate, primarily influenced by the balance between the hydrophobic pentyl chain and the hydrophilic hydroxycarbamate group.
  • Comparison to Similar Compounds: When compared to other carbamate derivatives, pentyl N-hydroxycarbamate may show enhanced solubility characteristics owing to its specific structure.
  • Temperature Effects: Solubility may vary with temperature, typically increasing in warmer conditions due to increased molecular motion.

Overall, the solubility of pentyl N-hydroxycarbamate is a reflection of its molecular structure, allowing it to interact favorably with solvents that can support hydrogen bonding interactions. As with many organic compounds, the choice of solvent is crucial in determining how well it will dissolve.

Interesting facts

Interesting Facts About Pentyl N-Hydroxycarbamate

Pentyl N-hydroxycarbamate is a fascinating compound predominantly studied within the realm of organic synthesis and medicinal chemistry. Here are some intriguing details about this compound:

  • Structure and Function: Pentyl N-hydroxycarbamate features a urethane functional group, which is critical in many biological applications. This structure allows it to interact effectively with various biological targets.
  • Biological Activity: Research indicates that compounds similar to pentyl N-hydroxycarbamate may exhibit significant biological activities, including anti-inflammatory properties, making them promising candidates for pharmaceutical development.
  • Synthesis: The synthesis of N-hydroxycarbamates generally involves the reaction of hydroxylamine with isocyanates. This flexible approach allows for various substitutions, leading to a range of biological applications.
  • Applications: Aside from its potential in medicine, this compound is also explored in agrochemicals, where it may affect plant growth or act as a pesticide through its influence on metabolic pathways.
  • Research Opportunities: The study of pentyl N-hydroxycarbamate opens doors to numerous research avenues including:
    • Development of novel drug formulations
    • Investigation of enzyme inhibition mechanisms
    • Exploration of the compound's role in polymer science

In summary, pentyl N-hydroxycarbamate holds considerable promise in various fields due to its unique structure and biological relevance. As a scientist or student, exploring its properties can uncover new applications and insights into the behavior of similar chemical entities.

Synonyms
Pentyl hydroxycarbamate
590-06-7
Hydroxycarbamic acid pentyl ester
n-Pentyl N-hydroxycarbamate
CCRIS 5074
BRN 1855227
CARBAMIC ACID, HYDROXY-, PENTYL ESTER
SCHEMBL3899146
DTXSID00207734