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Phenyramidol

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Identification
Molecular formula
C9H11NO3
CAS number
15302-03-7
IUPAC name
ethyl N-(3-hydroxyphenyl)carbamate
State
State

At room temperature, it is in a solid state, specifically forming crystalline particles or powders.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.15
Boiling point (Celsius)
406.00
Boiling point (Kelvin)
679.15
General information
Molecular weight
181.19g/mol
Molar mass
181.1920g/mol
Density
1.2607g/cm3
Appearence

Ethyl N-(3-hydroxyphenyl)carbamate appears as a white to off-white crystalline solid. It is typically characterized by its specific crystalline structure and can be identified visually by this solid formation.

Comment on solubility

Solubility of Ethyl N-(3-hydroxyphenyl)carbamate

The solubility of ethyl N-(3-hydroxyphenyl)carbamate in various solvents can be intriguing due to its structural characteristics. Understanding its solubility can give insights into its applications and behaviors in different environments. Here are some key points regarding its solubility:

  • Polar Solvents: Ethyl N-(3-hydroxyphenyl)carbamate is expected to exhibit reasonable solubility in polar solvents such as water and methanol. This is attributed to the presence of the hydroxyl group which can form hydrogen bonds with the solvent.
  • Non-Polar Solvents: It is likely to be less soluble in non-polar solvents like hexane or benzene due to the lack of strong interactions.
  • Temperature Influence: Solubility can also be temperature-dependent. Increasing the temperature often enhances solubility for many organic compounds.
  • pH Effects: The solubility may vary with pH, as the ionization of the hydroxyl group can affect how well the compound interacts with the solvent.

In summary, the solubility of ethyl N-(3-hydroxyphenyl)carbamate is influenced by its chemical structure and the nature of the solvent. As with many organic compounds, exploring the conditions under which maximal solubility occurs is essential for practical applications.

Interesting facts

Interesting Facts About Ethyl N-(3-Hydroxyphenyl)carbamate

Ethyl N-(3-hydroxyphenyl)carbamate is a fascinating compound that has garnered attention in various fields of science. Here are some intriguing aspects of this compound:

  • Pharmaceutical Applications: This compound is often explored for its potential in drug development, especially in the realm of anti-inflammatory and antioxidant therapies. The presence of the phenolic group plays a pivotal role in its biological activity.
  • Versatile Synthesis: Ethyl N-(3-hydroxyphenyl)carbamate can be synthesized through a variety of methods, showcasing the versatility of organic synthesis techniques. Researchers employ different catalytic systems to achieve desired yields and purities.
  • Role as a Building Block: In many organic synthesis pathways, this compound serves as a significant building block for the \emph{design and synthesis} of more complex structures, which include various pharmaceuticals and bioactive molecules.
  • Hydroxyphenyl Influence: The hydroxy group on the aromatic ring enhances the compound's water solubility and offers specific interaction sites for biological systems, making it an interesting target for further study in medicinal chemistry.
  • Environmental Perspectives: The compound's derivatives are also being investigated for their possible application in environmental chemistry, particularly in assessing the biodegradability and ecological impact of synthetic compounds.

In summary, ethyl N-(3-hydroxyphenyl)carbamate is not just a simple chemical compound; it is a prime example of how the intricate relationships between structure and function can lead to innovative advancements in scientific research across multiple disciplines.

Synonyms
Carbamic acid, N-(3-hydroxyphenyl)-, ethyl ester
Ethyl (3-hydroxyphenyl)carbamate
7159-96-8
Ethyl N-(3-hydroxyphenyl)carbamate
Ethyl 3-hydroxyphenylcarbamate
3-Carbethoxyaminophenol
Ethyl m-hydroxycarbanilate
Ethyl 3-hydroxycarbanilate
(3-Hydroxyphenyl)carbamic acid ethyl ester
m-Hydroxycarbanilic acid ethyl ester
(3-HYDROXY-PHENYL)-CARBAMIC ACID ETHYL ESTER
Carbamic acid, (3-hydroxyphenyl)-, ethyl ester
3-Ethyloxycarbonylaminophenol
4X2HYG86P1
NSC-222551
m-(Ethoxycarbonylamino)phenol
3-(Ethoxycarbonylamino)phenol
(3-Hydroxyphenyl)carbamic Acid Ethyl Ester;
NSC 222551
BRN 0909644
UNII-4X2HYG86P1
CARBANILIC ACID, m-HYDROXY-, ETHYL ESTER
MFCD00463773
Desmedipham metabolite
ethyl 3-hydroxycarbamate
Enamine_005305
EC 615-309-1
Oprea1_437556
1-13-00-00134 (Beilstein Handbook Reference)
SCHEMBL1933135
DTXSID6064581
KCLZXXMMEDEBMF-UHFFFAOYSA-N
HMS1409B03
HAA15996
ethyl-N-(3-hydroxyphenyl)-carbamate
Ethyl-N-(3-hydroxyphenyl)-carbamate ethyl 3-hydroxyphenylcarbamate
NSC222551
AKOS000118532
AS-60990
CS-0116794
E1227
NS00005873
EN300-05447
T72868
SR-01000405603
SR-01000405603-1
Q27260621
Z31717081