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p-Tolyl N-phenylcarbamate

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Identification
Molecular formula
C14H13NO2
CAS number
22542-43-0
IUPAC name
p-tolyl N-phenylcarbamate
State
State

At room temperature, p-Tolyl N-phenylcarbamate is in a solid state.

Melting point (Celsius)
97.00
Melting point (Kelvin)
370.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
213.26g/mol
Molar mass
213.2420g/mol
Density
1.1300g/cm3
Appearence

p-Tolyl N-phenylcarbamate is typically a crystalline solid. It can appear as off-white to pale-yellow crystals or powder.

Comment on solubility

Solubility of p-tolyl N-phenylcarbamate

The solubility of p-tolyl N-phenylcarbamate in various solvents can vary significantly due to its unique chemical structure. Understanding its solubility is crucial in many applications, including pharmaceutical formulations and chemical syntheses. Here are some key points regarding the solubility of this compound:

  • Polar Solvents: p-tolyl N-phenylcarbamate may exhibit limited solubility in highly polar solvents such as water due to the hydrophobic nature of the aromatic rings.
  • Non-Polar Solvents: The compound is more likely to dissolve in non-polar organic solvents, such as hexane and toluene, owing to similar interactions between the solvent and solute.
  • Intermediate Solvents: Solvents like ethanol or acetone may offer a moderate degree of solubility. This is attributed to their ability to engage in both polar and non-polar interactions.

In practical terms, solubility can be influenced by factors such as temperature and the presence of other solutes in the solution. As a general observation, one might note that:

  • Increased temperatures typically enhance solubility for many organic compounds.
  • The presence of functional groups in the solvent can also affect solubility patterns.

In conclusion, while p-tolyl N-phenylcarbamate shows variable solubility, understanding the solvent properties and environmental conditions is essential for effective application in scientific endeavors. As noted, "the solubility of a compound is as critical as its structure." Exploring these interactions can lead to innovative solutions in chemical research.

Interesting facts

Exploring p-Tolyl N-phenylcarbamate

p-Tolyl N-phenylcarbamate is a noteworthy compound in the realm of organic chemistry, particularly due to its applications and properties that contribute to various fields. Here are some intriguing insights:

  • Functional Versatility: This compound serves as a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals, showcasing its importance in the chemical industry.
  • Mechanism of Action: p-Tolyl N-phenylcarbamate exhibits potential for functioning as a pesticide. Its ability to inhibit certain enzymes makes it effective against a range of pests, which is crucial for enhancing agricultural yield.
  • Structural Diversity: The presence of both a tolyl group and a phenyl group in its structure contributes to unique electronic and steric properties, making it an interesting compound for chemical research and development.
  • Environmental Impact: Understanding the degradation pathways for this compound is fundamental for assessing its environmental impact and developing safer chemical alternatives.

As noted by renowned chemists, "The pursuit of chemical innovation is deeply intertwined with understanding complex compounds like p-tolyl N-phenylcarbamate." This highlights how studying compounds, regardless of their complexity, reveals pathways toward advancements in both science and industry.

In summary, p-tolyl N-phenylcarbamate exemplifies the intricate balance of ecological and industrial implications in chemistry. Its potential applications and the necessity of further study make it a compelling subject for both students and seasoned researchers alike.

Synonyms
CARBANILIC ACID, P-TOLYL ESTER
82BN83WRW2
4-methylphenyl N-phenylcarbamate
(4-methylphenyl) N-phenylcarbamate
CRESYL CARBANILATE, P-
DTXSID00167541
CARBAMIC ACID, N-PHENYL-, 4-METHYLPHENYL ESTER
DTXCID1090032
16323-13-0
Enamine_005719
UNII-82BN83WRW2
MLS001005689
SCHEMBL1376459
SCHEMBL6037493
CHEMBL1368480
HMS1410D21
HMS2733I21
AKOS001026730
IDI1_007954
NCGC00245991-01
SMR000348980
SR-01000402546
SR-01000402546-1
Z55290432