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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
methyl N-(1-phenylethylamino)carbamate
State
State

The compound is solid at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2220g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a colorless to white crystalline solid. However, the color can vary slightly to off-white depending on purity and environmental exposure. It is odorless with a characteristic mild chemical smell that is common to many carbamates.

Comment on solubility

Solubility of Methyl N-(1-phenylethylamino)carbamate

Methyl N-(1-phenylethylamino)carbamate is characterized by its solubility properties, which are crucial for its application in various fields. The solubility of this compound can be influenced by several factors, including:

  • Polarity: With functional groups such as amines and carbamates, this compound exhibits moderate polarity, enhancing solubility in polar solvents.
  • pH Levels: The ionization of the amine group can vary with pH, affecting its solubility in water and other solvents.
  • Temperature: Increasing temperatures often increase solubility in solvents; thus, varying temperature conditions can lead to different solubility outcomes.

While the precise solubility data for methyl N-(1-phenylethylamino)carbamate may not be extensively documented, it is commonly soluble in:

  • Polar Aprotic Solvents: Such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF).
  • Water: Moderate solubility can be expected due to the presence of polar functional groups, allowing it to dissolve to some extent.

In practical applications, knowing the solubility helps in predicting the behavior of methyl N-(1-phenylethylamino)carbamate in pharmaceutical formulations and chemical reactions. As the saying goes, "like dissolves like," emphasizing the significance of molecular interactions in determining solubility. Understanding these factors can assist researchers in optimizing the use of this compound in various systems.

Interesting facts

Interesting Facts about Methyl N-(1-phenylethylamino)carbamate

Methyl N-(1-phenylethylamino)carbamate is a fascinating compound in the realm of organic chemistry, primarily recognized for its role as a versatile building block in the synthesis of various pharmaceuticals. Here are some engaging insights:

  • Medicinal Chemistry: This compound is a part of a larger class of molecules known as carbamates, which are often utilized in the development of medicaments. Carbamates can exhibit a broad range of biological activities, making them a valuable subject of study.
  • Structure-Activity Relationship (SAR): The unique structure of methyl N-(1-phenylethylamino)carbamate allows chemists to explore the effects of substitutions on pharmaceutical efficacy. Small changes in its structure can lead to significant alterations in activity.
  • Potential Applications: Compounds like methyl N-(1-phenylethylamino)carbamate are often investigated for applications in treatments for a variety of conditions, including neurological disorders. The presence of the phenylethylamine moiety is particularly noteworthy because it resembles structures found in neurotransmitters, potentially influencing mood and cognition.
  • Research Significance: Researchers are constantly exploring the reactivity of carbamates. Methyl N-(1-phenylethylamino)carbamate can serve as a precursor in chemical reactions, allowing scientists to synthesize more complex compounds.

In summary, methyl N-(1-phenylethylamino)carbamate is not just a chemical formula; it represents an exciting intersection of medicinal chemistry and organic synthesis. Its potential applications and the insights it offers into molecular behavior make it a captivating topic for both students and professionals in the field.

Synonyms
7342-58-7
BRN 0746390
Methyl (3-(alpha-methyl)benzyl)carbazate
Carbamic acid, (alpha-methylbenzylamino)-, methyl ester
CARBAZIC ACID, 3-(alpha-METHYLBENZYL)-, METHYL ESTER
4-15-00-01268 (Beilstein Handbook Reference)
DTXSID10994143
Methyl hydrogen (1-phenylethyl)carbonohydrazonate