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Bendiocarb

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Identification
Molecular formula
C11H13NO4S
CAS number
22781-23-3
IUPAC name
(3,5-dimethyl-4-methylsulfonyl-phenyl) N-methylcarbamate
State
State

At room temperature, Bendiocarb is a solid. It is commonly used in powdered or crystalline form.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
335.80
Boiling point (Kelvin)
608.95
General information
Molecular weight
223.30g/mol
Molar mass
223.2670g/mol
Density
1.2320g/cm3
Appearence

Bendiocarb is a white crystalline solid with no distinct odor. It is typically utilized in its solid form for various applications.

Comment on solubility

Solubility of (3,5-dimethyl-4-methylsulfonyl-phenyl) N-methylcarbamate

The solubility characteristics of (3,5-dimethyl-4-methylsulfonyl-phenyl) N-methylcarbamate can offer valuable insights into its potential applications and behaviors in various environments. Understanding how this compound interacts with solvents is essential for effective use in both industrial and research settings.

Key Factors Affecting Solubility:

  • Molecular Structure: The presence of functional groups such as the methylsulfonyl group can significantly influence solubility.
  • Polarity: Due to the arrangement of hydrophilic and hydrophobic parts in the structure, the solubility may vary between polar and nonpolar solvents.
  • Temperature: As with many compounds, an increase in temperature often leads to greater solubility.

In general, it is suggested that:

  • The compound may exhibit enhanced solubility in polar solvents due to potential hydrogen bonding and dipole-dipole interactions.
  • Organic solvents such as methanol or dimethyl sulfoxide (DMSO) might be effective in dissolving this compound.
  • It can be less soluble in nonpolar solvents due to its polar substituents.

Research findings and experimental data will provide the most accurate determination of solubility. As stated, "The solubility of a compound can reveal much about its potential applications in pharmacology and agrochemicals." Thus, understanding the solubility profile of (3,5-dimethyl-4-methylsulfonyl-phenyl) N-methylcarbamate is crucial for harnessing its full potential.

Interesting facts

Interesting Facts about (3,5-dimethyl-4-methylsulfonyl-phenyl) N-methylcarbamate

(3,5-dimethyl-4-methylsulfonyl-phenyl) N-methylcarbamate is an intriguing compound that finds its niche primarily in the realm of organic chemistry and agrochemicals. This compound is notable for its structural composition and potential applications, making it a topic of study for chemists and researchers alike.

Key Features

  • Functional Groups: This compound contains a carbamate functional group, which is significant in medicinal chemistry for its versatility in drug design.
  • Methylsulfonyl Group: The presence of a methylsulfonyl moiety not only enhances its chemical reactivity but also influences the compound's biological activity.
  • Dimethyl Substitution: The dimethyl substitutions on the aromatic ring can impact the compound's interaction with biological systems, providing interesting avenues for research.

Applications

Research indicates that compounds featuring carbamate structures are often investigated for their insecticidal and herbicidal properties. In particular, this compound could be of interest for temporary pest management solutions in agriculture.

Scientific Insights

One fascinating aspect of (3,5-dimethyl-4-methylsulfonyl-phenyl) N-methylcarbamate is its potential to serve as a lead compound in drug discovery. As noted by many chemists, compounds in the carbamate class often exhibit bioactivity, which lays the groundwork for their utilization in therapeutic applications.

In the words of a renowned chemist, "The future of organic synthesis lies in understanding how small modifications can lead to significant changes in functionality."

This compound serves as a perfect example of this philosophy, making it a valuable subject for ongoing studies in both academic and industrial chemistry settings.

Synonyms
Methiocarb sulfone
2179-25-1
Mesurol sulfone
Mercaptodimethursulfon
Bayer 37344 sulfone
BAY 37344 sulfone
U9FTK96C2O
BAY 41790
ENT 25825
Phenol, 3,5-dimethyl-4-(methylsulfonyl)-, methylcarbamate
METHIOCARB SULPHONE
BA 51-084786
UNII-U9FTK96C2O
3,5-Xylenol, 4-(methylsulfonyl)-, methylcarbamate
BRN 2291460
AI3-25825
BAY-37344 SULFONE
DTXSID3042138
Carbamic acid, methyl-, 3,5-dimethyl-4-(methylsulfonyl)phenyl ester
CARBAMIC ACID, METHYL-, 4-(METHYLSULFONYL)-3,5-XYLYL ESTER
BAY-41790
4-methanesulfonyl-3,5-dimethylphenyl N-methylcarbamate
3,5-DIMETHYL-4-(METHYLSULFONYL)PHENOL METHYLCARBAMATE
PHENOL, 3,5-DIMETHYL-4-(METHYLSULFONYL)-, 1-(N-METHYLCARBAMATE)
DTXCID1022138
3,5-Dimethyl-4-(methylsulfonyl)phenyl methylcarbamate
Phenol, 3,5-dimethyl-4-(methylsulfonyl)-, methylcarbamate (9CI)
rjbjmkamqioaml-uhfffaoysa-n
(3,5-dimethyl-4-methylsulfonylphenyl) N-methylcarbamate
Methiocarb-sulfone
Methiocarb-sulfone 100 microg/mL in Methyl-tert-butyl ether
Methiocarb M02
SCHEMBL5933707
MSK20264
AKOS015888399
Methiocarb sulfone, analytical standard
NS00002491
Methiocarb sulfone, PESTANAL(R), analytical standard
Q27290955
3,5-Dimethyl-4-(methylsulfonyl)phenyl methylcarbamate #