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Benzyl N-(3-hydroxyphenyl)carbamate

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Identification
Molecular formula
C14H13NO3
CAS number
93951-73-2
IUPAC name
benzyl N-(3-hydroxyphenyl)carbamate
State
State

At room temperature, benzyl N-(3-hydroxyphenyl)carbamate is typically a crystalline solid.

Melting point (Celsius)
124.00
Melting point (Kelvin)
397.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
243.27g/mol
Molar mass
243.2660g/mol
Density
1.2760g/cm3
Appearence

Benzyl N-(3-hydroxyphenyl)carbamate generally appears as a crystalline solid, although the exact color may vary based on impurities or particular synthesis methods. It is often white to off-white in appearance.

Comment on solubility

Solubility of Benzyl N-(3-hydroxyphenyl)carbamate

Benzyl N-(3-hydroxyphenyl)carbamate, a compound with the formula C14H15NO3, exhibits an intriguing solubility profile that is influenced by its structural characteristics.

In terms of solubility, it is essential to consider several key factors:

  • Polarity: The presence of the hydroxyl group (-OH) in the molecule increases polarity, suggesting that benzyl N-(3-hydroxyphenyl)carbamate may demonstrate better solubility in polar solvents.
  • Solvent Compatibility: This compound is likely more soluble in solvents such as methanol and ethanol, while exhibiting limited solubility in non-polar solvents like hexane.
  • Temperature Effects: As with many organic compounds, solubility can improve with an increase in temperature, making hot solvents more effective for dissolving the compound.
  • pH Influence: The solubility may also be affected by pH, as the protonation of the hydroxyl group in acidic conditions could alter interactions with the solvent.

To sum up, the solubility of benzyl N-(3-hydroxyphenyl)carbamate varies according to solvent choice and environmental conditions, making it essential to consider these factors in practical applications. Understanding its solubility can significantly influence its usage in various chemical processes and formulations.

Interesting facts

Interesting Facts about Benzyl N-(3-Hydroxyphenyl)carbamate

Benzyl N-(3-hydroxyphenyl)carbamate is a fascinating compound that attracts attention for its unique structural features and potential applications. Below are several intriguing aspects of this compound:

  • Biological Relevance: This compound can be studied in the context of medicinal chemistry. Its structure suggests potential interactions with biological targets, making it a candidate for research in drug development.
  • Functional Groups: The presence of both a carbamate group and a hydroxyphenyl substituent can contribute to interesting chemical reactivity. Carbamates are known for their roles in pharmaceuticals and agrochemicals.
  • Synthetic Utility: Benzyl N-(3-hydroxyphenyl)carbamate may serve as an intermediate in the synthesis of more complex organic molecules. Its derivatives might find utility in creating novel materials or drug scaffolds.
  • Research Applications: Compounds like this one are often investigated for their antioxidant and anti-inflammatory properties, making them potential agents in combating various diseases.
  • Structural Insights: The configuration of benzyl and hydroxyphenyl groups not only plays a role in the compound's stability but also influences its solubility and reactivity in different environments.

As scientists continue to explore the multitude of applications and functions of benzyl N-(3-hydroxyphenyl)carbamate, it remains a prime example of how organic chemistry can intersect with biology and materials science. The possibilities are both varied and exciting, paving the way for future innovations!

Synonyms
19972-88-4
Benzyl m-hydroxycarbanilate
Carbamic acid, (3-hydroxyphenyl)-, phenylmethyl ester (9CI)
m-Hydroxycarbanilic acid benzyl ester
Phenylmethyl (3-hydroxyphenyl)carbamate
BRN 4451293
CARBANILIC ACID, m-HYDROXY-, BENZYL ESTER
Carbamic acid, (3-hydroxyphenyl)-, phenylmethyl ester
DTXSID90173772
DTXCID6096263
RefChem:332043
benzyl N-(3-hydroxyphenyl)carbamate
orb1986316
SCHEMBL8984657
SCHEMBL27924561
AKOS029899194
EN300-7243439