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Allyl 3-chlorophenylcarbamate

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Identification
Molecular formula
C10H10ClNO2
CAS number
6775-55-7
IUPAC name
allyl N-(3-chlorophenyl)carbamate
State
State

At room temperature, allyl 3-chlorophenylcarbamate is a solid.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
211.65g/mol
Molar mass
211.6350g/mol
Density
1.1580g/cm3
Appearence

Allyl 3-chlorophenylcarbamate appears as a pale or colorless crystalline solid. It may also appear as a powder.

Comment on solubility

Solubility of Allyl N-(3-chlorophenyl)carbamate

The solubility of allyl N-(3-chlorophenyl)carbamate is an intriguing aspect that can greatly affect its applications in various fields. Understanding its solubility characteristics involves considering several factors:

  • Polarity: The presence of both the allyl group and the chlorophenyl moiety suggests that the compound has significant polarity, impacting its interaction with different solvents.
  • Solvent compatibility: This compound may exhibit varying solubility in:
    • Water: Generally low due to the hydrophobic nature of the aromatic ring.
    • Organic solvents: Likely higher solubility in non-polar solvents such as hexane or chloroform.
    • Polar aprotic solvents: May dissolve better in solvents like acetone or DMSO.
  • Concentration effects: The solubility may also vary with concentration; at higher concentrations, precipitation may occur.

Understanding these solubility dynamics is crucial for applications such as formulation in pharmaceuticals, agricultural chemistry, or materials science. Thus, one might conclude that while the solubility of allyl N-(3-chlorophenyl)carbamate could be limited in aqueous environments, it possesses favorable characteristics for use in organic systems.

Interesting facts

Interesting Facts About Allyl N-(3-Chlorophenyl)carbamate

Allyl N-(3-chlorophenyl)carbamate is a fascinating compound with noteworthy applications in various fields. Here are some key points that illustrate its significance:

  • Versatile Use: This compound is primarily utilized in the synthesis of pharmaceutical agents, particularly those that act as insecticides and herbicides. Its structure allows for a wide range of chemical modifications, enhancing its utility in agrochemicals.
  • Mechanism of Action: The compound works by interfering with the nervous systems of pests, thereby acting as an effective pest control agent. This mode of action highlights its importance in sustainable agriculture and environmental protection.
  • Synthetic Pathways: Chemists often explore various synthetic routes to create allyl N-(3-chlorophenyl)carbamate, emphasizing its structural complexity. This includes approaches like amine coupling and carbamate formation, showcasing valuable skills in organic synthesis.
  • Research Interest: Due to its specific structural characteristics, it serves as a subject of interest for ongoing research aimed at developing new pest control methods that are both effective and environmentally friendly. "Innovation in chemistry drives sustainable solutions," a motto echoed in research labs worldwide.
  • Safety Profile: Understanding the toxicological profile of this compound is crucial. Research into its safety ensures that it can be used effectively without harming non-target organisms, making it a safer choice in agricultural practices.

In summary, allyl N-(3-chlorophenyl)carbamate exemplifies the intersection of chemistry and environmental stewardship. Its diverse applications, from agrochemicals to research avenues, prove that the world of chemical compounds offers profound insights and advancements in modern science.

Synonyms
25070-79-5
m-Chlorophenylcarbamic acid allyl ester
NYF9ZD4NKW
CARBANILIC ACID, m-CHLORO-, ALLYL ESTER
NSC 29689
BRN 3267809
Carbamic acid, m-chlorophenyl-, allyl ester
NSC-29689
DTXSID40179764
2-PROPEN-1-YL N-(3-CHLOROPHENYL)CARBAMATE
CARBAMIC ACID, N-(3-CHLOROPHENYL)-, 2-PROPEN-1-YL ESTER
RefChem:574148
DTXCID00102255
prop-2-enyl N-(3-chlorophenyl)carbamate
Allyl (3-chlorophenyl)carbamate
UNII-NYF9ZD4NKW
WLN: GR CMVO2UU1
allyl 3-chlorophenylcarbamate
SCHEMBL7011472
Carbamic acid,N-(3-chlorophenyl)-, 2-propen-1-yl ester
AKUHKJFFZQUCEH-UHFFFAOYSA-N
NSC29689
AKOS024335035
DS-007454
Carbamic acid, 3-chlorophenyl-, allyl ester