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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[3-(3-methylbut-2-enoylamino)phenyl] N-methylcarbamate
State
State

Carbaryl is generally encountered in a solid state at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
315.60
Boiling point (Kelvin)
588.75
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is typically found as a white crystalline solid. It does not have any odor, making it relatively easy to handle in controlled environments.

Comment on solubility

Solubility Profile of [3-(3-methylbut-2-enoylamino)phenyl] N-methylcarbamate

The solubility of [3-(3-methylbut-2-enoylamino)phenyl] N-methylcarbamate can be influenced by various factors including its molecular structure, polarity, and the presence of functional groups. Understanding its solubility is crucial for applications in pharmaceutical formulations and chemical processes.

Factors Affecting Solubility:

  • Molecular Polarity: The presence of polar functional groups (e.g., the carbamate group) can enhance solubility in polar solvents like water.
  • Hydrophobic Regions: The non-polar alkyl chains may cause reduced solubility in aqueous environments, indicating potential amphiphilic behavior.
  • Temperature: Solubility generally increases with temperature; thus, evaluating solubility across varying temperatures can provide more insights.

It is important to note that while [3-(3-methylbut-2-enoylamino)phenyl] N-methylcarbamate may exhibit some solubility in organic solvents, specific quantitative solubility data should be referenced to assess its practical applications. Experimental determinations often yield better clarity on its solubility characteristics.

Interesting facts

Interesting Facts about [3-(3-methylbut-2-enoylamino)phenyl] N-methylcarbamate

[3-(3-methylbut-2-enoylamino)phenyl] N-methylcarbamate is a fascinating organic compound that beckons curiosity in the fields of chemistry and pharmacology. Here are some intriguing insights:

  • Structural Complexity: This compound features a unique structure that includes both an amino group and a carbamate moiety, making it particularly interesting for researchers studying reactive intermediates in organic synthesis.
  • Potential Pharmacological Applications: Due to its nitrogen-containing functional groups, it has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways.
  • Synthesis Pathways: The synthesis of this compound often involves multi-step reactions, showcasing the beautiful intricacies of organic synthesis and the importance of careful planning in chemical reactions.
  • Intermolecular Interactions: The presence of multiple functional groups allows for intriguing intermolecular interactions, which can be explored in various chemical environments, making it an interesting compound for studying solvation effects.
  • Insights into Substituent Effects: The 3-methylbut-2-enoyl group provides an opportunity to study steric and electronic effects in substituents, enhancing our understanding of reaction mechanisms.
  • Research Relevance: Compounds like this are often evaluated in drug discovery programs, providing valuable insights into the optimization of bioactive molecules.

In summary, [3-(3-methylbut-2-enoylamino)phenyl] N-methylcarbamate is not only a compound of structural interest but also poses numerous possibilities for practical applications in science and medicine. Its complexity showcases the deep interconnectedness between structure and function in the world of organic chemistry.

Synonyms
17798-18-4
m-(3-Methylcrotonamido)phenyl methylcarbamate
CROTONAMIDE, N-(m-HYDROXYPHENYL)-3-METHYL-, METHYLCARBAMATE
O6P7KK8TD8
N-(m-Hydroxyphenyl)-3-methylcrotonamide methylcarbamate
NSC-222541
2-Butenamide, 3-methyl-N-(3-(((methylamino)carbonyl)oxy)phenyl)-
3'-Hydroxy-3-methylcrotonanilide methylcarbamate
2-Butenamide, 3-methyl-N-[3-[[(methylamino)carbonyl]oxy]phenyl]-
NSC 222541
BRN 2128486
UNII-O6P7KK8TD8
Crotonamide, methylcarbamate
DTXSID90170408
WLN: 1Y1&U1VMR COVM1
NSC222541
CARBAMIC ACID, METHYL-, ESTER WITH 3'-HYDROXY-3-METHYLCROTONANILIDE
CROTONANILIDE, 3'-HYDROXY-3-METHYL-, METHYLCARBAMATE (ESTER)