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Chlorpropham

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Identification
Molecular formula
C10H12ClNO2
CAS number
101-21-3
IUPAC name
2-chloroethyl N-anilinocarbamate
State
State

At room temperature, chlorpropham is typically a solid substance. It is stable under normal temperatures and conditions.

Melting point (Celsius)
41.50
Melting point (Kelvin)
314.65
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
213.66g/mol
Molar mass
213.6600g/mol
Density
1.2203g/cm3
Appearence

Chlorpropham is a colorless to white crystalline solid. It may also appear as a solid powder or crystals depending on its preparation and storage conditions.

Comment on solubility

Solubility of 2-chloroethyl N-anilinocarbamate

The solubility characteristics of 2-chloroethyl N-anilinocarbamate can be quite fascinating. This compound, with its complex structure, exhibits varying degrees of solubility that are influenced by several factors:

  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents, whereas non-polar regions may hinder solubility in such environments.
  • Solvent Interaction: This compound is likely to have better solubility in organic solvents such as ethanol or acetone, compared to water due to its organic nature.
  • Temperature Dependence: Solubility can increase with temperature, making it essential to consider thermal conditions when dissolving this compound.
  • pH Sensitivity: The solubility may vary with pH changes; therefore, testing in different pH environments can provide more insight into behavior.

Overall, while 2-chloroethyl N-anilinocarbamate presents intriguing solubility traits, *experimental validation is essential to ascertain its solubility profile accurately.* Understanding its solubility not only helps in handling and application but also gives insights into its potential interactions in various chemical environments.

Interesting facts

Interesting Facts about 2-Chloroethyl N-Anilinocarbamate

2-Chloroethyl N-anilinocarbamate is a fascinating chemical compound that belongs to the class of carbamates. This compound has garnered attention for its unique properties and potential applications in various fields. Here are some noteworthy facts:

  • Mechanism of Action: 2-Chloroethyl N-anilinocarbamate functions as a carbamate pesticide. Its mode of action involves the inhibition of acetylcholinesterase, an essential enzyme for the proper functioning of synapses. This attribute makes it effective against pests while highlighting the importance of enzyme dynamics in biological processes.
  • Historical Context: Carbamates were developed as a synthetic alternative to organophosphates in the post-World War II era. These compounds initiated a new era in agricultural chemistry, contributing to food production enhancements while ensuring a certain level of environmental safety.
  • Potential Impact: Research continues to explore the potential uses of 2-chloroethyl N-anilinocarbamate in medicinal chemistry, particularly in the development of new therapeutic agents aimed at neurological disorders, where the modulation of acetylcholine is desirable.
  • Importance in Research: The compound serves as a model for studying structure-activity relationships (SAR) among carbamate compounds. Scientifically, this can assist researchers in designing better pesticides or pharmaceuticals tailored to specific biological targets.
  • Synthesis: The synthesis of this compound typically involves the reaction of chloroethylamine with aniline in the presence of appropriate reagents. Understanding the synthesis pathways is critical in organic chemistry and for the development of new compounds.

As you delve deeper into the world of 2-chloroethyl N-anilinocarbamate, it’s essential to consider both its potential benefits and risks. The balance between agricultural practices and environmental stewardship remains a pivotal discussion in the field of chemistry.


Synonyms
3-Phenylcarbazic acid 2-chloroethyl ester
5923-43-3
2-Chloroethyl N(sup2)-phenylcarbazate
CARBAZIC ACID, 3-PHENYL-, 2-CHLOROETHYL ESTER
2-Chloroethyl N(sup 2)-phenylcarbazate
NSC 43645
BRN 0646470
2-chloroethyl N-(anilino)carbamate
WLN: G2OVMMR
2-15-00-00106 (Beilstein Handbook Reference)
DTXSID80207974
Carbazic acid, 2-chloroethyl ester
NSC43645
NSC-43645
2-chloroethyl 2-phenylhydrazinecarboxylate
DB-228738
Hydrazinecarboxylic acid, 2-phenyl-, 2-chloroethyl ester