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sec-butyl N-(3-chlorophenyl)carbamate

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Identification
Molecular formula
C11H14ClNO2
CAS number
101-21-3
IUPAC name
sec-butyl N-(3-chlorophenyl)carbamate
State
State
The compound is typically in a solid state at room temperature, often found in crystalline form.
Melting point (Celsius)
42.00
Melting point (Kelvin)
315.15
Boiling point (Celsius)
307.00
Boiling point (Kelvin)
580.15
General information
Molecular weight
213.68g/mol
Molar mass
213.6810g/mol
Density
1.1690g/cm3
Appearence

The compound sec-butyl N-(3-chlorophenyl)carbamate typically appears as a white to off-white crystalline solid. The texture and color may vary slightly depending on the exact formulation and purity of the sample.

Comment on solubility

Solubility of sec-butyl N-(3-chlorophenyl)carbamate

The solubility of sec-butyl N-(3-chlorophenyl)carbamate can be influenced by several factors including temperature, pH, and solvent polarity. Here are some key points to consider:

  • Solvent Compatibility: This compound tends to be more soluble in organic solvents such as ethanol and acetone, reflecting its nonpolar hydrocarbon chain.
  • Temperature Effects: Increasing the temperature generally enhances solubility in solvents. It is advisable to conduct solubility tests at various temperatures to identify optimal conditions.
  • pH Influence: The solubility can significantly change with pH adjustments, especially if the compound has ionizable functional groups under different pH conditions.
  • Molecular Interactions: The presence of the 3-chlorophenyl moiety can contribute to strong intermolecular forces that may hinder solubility; hence, understanding these interactions is crucial.

It is often observed that "like dissolves like," meaning the polarities of the solute and solvent should be considered for effective dissolution. Careful selection of conditions can lead to enhanced solubility, facilitating the compound's applicability in various chemical processes.

Interesting facts

Interesting Facts about sec-butyl N-(3-chlorophenyl)carbamate

sec-butyl N-(3-chlorophenyl)carbamate is a fascinating compound that finds applications in various fields of chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Structure and Function: It features a sec-butyl group, which is notable in the world of organic compounds. This branched structure enhances its stability and allows for interesting interactions with other molecules.
  • Biological Significance: The presence of the 3-chlorophenyl group provides unique characteristics that can influence its reactivity and biological activity. Chlorinated phenyl rings are often associated with increased potency in various biological applications.
  • Use in Agriculture: Carbamates, a class that sec-butyl N-(3-chlorophenyl)carbamate belongs to, are commonly used as pesticides. Their efficacy in controlling pests makes them valuable in agricultural practices.
  • Mechanism of Action: Understanding the mode of action for compounds like sec-butyl N-(3-chlorophenyl)carbamate can lead to advancements in pesticide development by optimizing selective toxicity toward pests while minimizing impact on non-target species.
  • Research Potential: As scientists continue to explore the potential applications of this compound, the insights gained from studying its interactions could contribute to the development of novel therapeutic agents or environmentally friendly agricultural solutions.

In conclusion, sec-butyl N-(3-chlorophenyl)carbamate is not just a chemical compound; it represents the intricate balance between structure and function that modern chemistry seeks to understand and harness. The exploration of its potential could lead to significant breakthroughs in both health and agriculture, demonstrating the ongoing importance of chemical research in our society.

Synonyms
BCPC
2164-13-8
sec-Butyl N-(3-chlorophenyl)carbamate
BCPC [ISO]
BP 9
2N91I87D2B
NSC-2475
NSC-74793
Carbanilic acid, sec-butyl ester
butan-2-yl N-(3-chlorophenyl)carbamate
UNII-2N91I87D2B
BP-9
SCHEMBL1412533
Carbamic acid,N-(3-chlorophenyl)-, 1-methylpropyl ester
DTXSID90874212
NSC2475
NSC 2475
NSC74793
NSC 74793
DS-007453
Carbanilic acid, m-chloro-, sec-butyl ester
SEC-BUTYL ALCOHOL, M-CHLOROCARBANILATE
Q27255098
CARBAMIC ACID, N-(3-CHLOROPHENYL)-, 1-METHYLPROPYL ESTER