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Felbamate

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Identification
Molecular formula
C11H14ClNO4
CAS number
25451-15-4
IUPAC name
1-(2-chlorophenyl)propyl carbamate
State
State

Felbamate is a solid at room temperature.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
332.00
Boiling point (Kelvin)
605.15
General information
Molecular weight
238.68g/mol
Molar mass
238.6840g/mol
Density
1.2070g/cm3
Appearence

Felbamate is a white to off-white crystalline powder. It is relatively odorless and tasteless, which makes it suitable for pharmaceutical formulations.

Comment on solubility

Solubility of 1-(2-chlorophenyl)propyl carbamate

The solubility of 1-(2-chlorophenyl)propyl carbamate is influenced by various interplaying factors such as its molecular structure, polarity, and the surrounding solvent environment. Typically, you can expect:

  • Polarity: Due to the presence of the carbamate functional group, 1-(2-chlorophenyl)propyl carbamate tends to exhibit polar characteristics, which often leads to greater solubility in polar solvents.
  • Solvent Interaction: This compound may show improved solubility in protic solvents, like water, compared to aprotic solvents.
  • Temperature Influence: As with many organic compounds, solubility can increase with rising temperature; thus, higher temperatures may enhance its dissolution in chosen solvents.

In general, while specific quantitative solubility data may vary, understanding that the 2-chlorophenyl group adds to both polarity and potential interactions with various solvents is critical. As always, consulting experimental data and solubility charts will provide the most accurate information for practical applications.

Interesting facts

Interesting Facts about 1-(2-chlorophenyl)propyl carbamate

The compound 1-(2-chlorophenyl)propyl carbamate, also known for its role in various chemical applications, has garnered interest in both industry and laboratory settings. Here are some fascinating points regarding this compound:

  • Pesticide Applications: This compound is often investigated for its potential use as a pesticide. Its structure facilitates interaction with specific biological targets, showcasing the importance of chemistry in agriculture.
  • Mechanism of Action: The mechanism of action in biological systems is essential for understanding its effects. Compounds in this category may inhibit enzymes critical for pest survival, making them effective in controlling agricultural pests.
  • Chiral Centers: The presence of a chiral center in its structure can lead to the generation of enantiomers, which may exhibit different biological activities. This introduces a fascinating topic in stereochemistry and its implications in pharmacology.
  • Environmental Impact: Research is ongoing regarding the environmental persistence of carbamate compounds. Understanding their degradation and potential accumulation in ecosystems is vital for sustainable agricultural practices.
  • Potential for Improvement: The fine-tuning of the compound's chemical properties is an area of active research. Chemists are exploring structural modifications to enhance efficacy and minimize environmental impact.

In the realm of organic chemistry, compounds like 1-(2-chlorophenyl)propyl carbamate serve as examples of how molecular structure influences function. As a chemist keen on pursuing sustainable solutions, one might contemplate how such compounds can evolve to meet modern agricultural needs while preserving ecological balance.

Synonyms
1-(2-chlorophenyl)propyl carbamate
1690-33-1
Carbamic acid o-chloro-alpha-ethylbenzyl ester
MH 586
o-Chloro-alpha-ethylbenzyl carbamate
BRN 1877589
CARBAMIC ACID, o-CHLORO-alpha-ETHYLBENZYL ESTER
DTXSID50937574
1-(2-Chlorophenyl)propyl hydrogen carbonimidate