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Carbaryl

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Identification
Molecular formula
C12H11NO3
CAS number
63-25-2
IUPAC name
1,3-benzodioxol-5-yl N-methylcarbamate
State
State
At room temperature, carbaryl is a solid compound, commonly found in a crystalline form.
Melting point (Celsius)
142.50
Melting point (Kelvin)
415.60
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.00
General information
Molecular weight
201.22g/mol
Molar mass
201.2200g/mol
Density
1.2300g/cm3
Appearence
Carbaryl typically appears as a white crystalline solid. It is odorless or may have a faint chemical smell.
Comment on solubility

Solubility of 1,3-benzodioxol-5-yl N-methylcarbamate

The solubility of 1,3-benzodioxol-5-yl N-methylcarbamate can be characterized by several important factors:

  • Polarity: This compound contains both polar and nonpolar functional groups, influencing its solubility in various solvents.
  • Solvent Types: It is likely to be more soluble in polar organic solvents such as ethanol or methanol, while displaying limited solubility in nonpolar solvents like hexane.
  • Temperature Effects: As is common with many compounds, solubility may increase with temperature, enhancing the ability to dissolve in a solvent.

Understanding the solubility behavior of this compound is essential, as it affects aspects such as bioavailability, reactions in solution, and application in various environments. The interplay between solubility and these factors showcases the nuanced behavior of organic compounds in chemical processes.

Interesting facts

Interesting Facts about 1,3-Benzodioxol-5-yl N-methylcarbamate

The compound 1,3-benzodioxol-5-yl N-methylcarbamate, often referred to in scientific circles for its structural complexity, belongs to the class of carbamate compounds. This compound is recognized for its unique molecular architecture, which consists of a benzodioxole ring fused with a carbamate group, leading to intriguing biological activities.

Biological Significance

  • Potential Pharmacological Uses: This compound has drawn interest due to its potential pharmacological effects, particularly in the fields of neuropharmacology and medicinal chemistry.
  • Inhibition Studies: Preliminary studies suggest that it may exhibit inhibitory effects on certain enzymes, which can pave the way for the development of novel therapeutic agents.
  • Natural Products Chemistry: Its structure is similar to various naturally occurring compounds, indicating a potential source for bioactive substances.

Structure and Stability

The distinct 1,3-benzodioxole structure lends this compound favorable stability compared to other more traditional carbamates. This enhanced stability is attributed to intramolecular interactions that could impact its reactivity and solubility characteristics.

Chemical Characteristics

  • Reactivity: As a carbamate, it can participate in various chemical reactions, making it a valuable intermediate in organic synthesis.
  • Versatile Derivatives: The ability to modify the N-methyl group can lead to a variety of derivatives, potentially expanding its utility in research and industry.

In summary, 1,3-benzodioxol-5-yl N-methylcarbamate is a fascinating compound with a promising future in scientific research. Its complex structure and potential biological activities make it a worthwhile subject for further study and exploration in pharmaceuticals and chemical synthesis.

Synonyms
1,3-Benzodioxol-5-ol, methylcarbamate
3,4-Methylenedioxyphenyl methylcarbamate
120-60-5
PKR64R31AF
NSC 50221
BRN 1347880
NSC-50221
UNII-PKR64R31AF
CARBAMIC ACID, METHYL-, 3,4-METHYLENEDIOXYPHENYL ESTER
DTXSID70152646
5-19-02-00533 (Beilstein Handbook Reference)
1,3-BENZODIOXOL-5-OL, 5-(N-METHYLCARBAMATE)
CARBAMIC ACID, METHYL-, 3,4-(METHYLENEDIOXY)PHENYL ESTER
DTXCID7075137
SCHEMBL11695674
NSC50221