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Bendiocarb

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Identification
Molecular formula
C11H13NO4
CAS number
22781-23-3
IUPAC name
(3-sec-butylphenyl) N-methyl-N-(2-phenoxyacetyl)carbamate
State
State

At room temperature, Bendiocarb is in a solid state. It exists as a crystalline powder that does not readily evaporate or sublimate.

Melting point (Celsius)
121.00
Melting point (Kelvin)
394.00
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.00
General information
Molecular weight
223.27g/mol
Molar mass
223.2660g/mol
Density
1.1869g/cm3
Appearence

Bendiocarb is typically a white crystalline solid. It is odorless and usually comes in a technical grade that ranges from 95 to 97% purity. When inspecting the material, it is notably free of lumps or discolorations.

Comment on solubility

Solubility of (3-sec-butylphenyl) N-methyl-N-(2-phenoxyacetyl)carbamate

The solubility of the compound (3-sec-butylphenyl) N-methyl-N-(2-phenoxyacetyl)carbamate can be influenced by several factors, making it a fascinating subject of study. Here are some key points to consider:

  • Polarity: The presence of both hydrophobic (the sec-butyl and phenyl groups) and hydrophilic (the carbamate and phenoxyacetyl moieties) components suggests that the compound may exhibit moderate solubility in organic solvents.
  • Organic Solvents: Common solvents may include:
    • Dimethyl sulfoxide (DMSO)
    • Acetone
    • Ethanol
  • Aqueous Solubility: While the compound might have limited solubility in water due to its bulky groups, interactions with water could enhance solubility under certain conditions.
  • Temperature Dependence: The solubility may increase with temperature, a typical behavior for many organic compounds as kinetic energy increases.

In summary, studying the solubility characteristics of (3-sec-butylphenyl) N-methyl-N-(2-phenoxyacetyl)carbamate could reveal insights into its behavior in various environments, influencing its applications and efficacy in different settings.

Interesting facts

Interesting Facts About (3-sec-butylphenyl) N-methyl-N-(2-phenoxyacetyl)carbamate

(3-sec-butylphenyl) N-methyl-N-(2-phenoxyacetyl)carbamate is a fascinating compound that falls under the category of carbamates, which are esters or salts of carbamic acid. This chemical structure offers various intriguing characteristics:

  • Pharmacological Potential: This compound showcases properties that make it essential in pharmaceutical applications, particularly in the development of drugs that target specific biological pathways.
  • Insecticidal Applications: Many carbamates are known for their insecticidal properties, functioning as neurotoxins to pests. This compound’s structural attributes may grant it potential usage in agricultural settings, enhancing crop protection.
  • Synthetic Versatility: The synthesis of this compound involves multiple organic reactions, providing a great platform for students and chemists to explore techniques like esterification and nucleophilic substitution.
  • Behavior in Biological Systems: Understanding how this compound interacts within biological entities can lead to advancements in toxicology and pharmacokinetics, influencing how similar compounds are designed and utilized.

As scientists continue to explore its properties, this compound not only presents challenges in understanding its full spectrum of effects but also opens doors for innovative applications in both medicinal chemistry and environmental science.

To quote a popular saying among chemists, “Where there’s a reaction, there’s a discovery.” This compound embodies that spirit of exploration and the potential for groundbreaking findings in chemical research.

Synonyms
16156-66-4
(3-butan-2-ylphenyl) N-methyl-N-(2-phenoxyacetyl)carbamate
Upjohn U-22024
Methyl(phenoxyacetyl)carbamic acid m-sec-butylphenyl ester
U-22024
ENT 27,352
NSC 190950
BRN 1893370
2-(1-Methylpropyl)phenyl methyl(phenoxyacetyl)carbamate
Carbamic acid, methyl(phenoxyacetyl)-, 2-(1-methylpropyl)phenyl ester
CARBAMIC ACID, METHYL(PHENOXYACETYL)-, m-sec-BUTYLPHENYL ESTER
DTXSID80936550
3-(Butan-2-yl)phenyl methyl(phenoxyacetyl)carbamate
(3-Butan-2-ylphenyl)n-methyl-N-[2-(phenoxy)acetyl]carbamate