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Methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate

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Identification
Molecular formula
C14H18ClNO3
CAS number
131-14-6
IUPAC name
methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate
State
State

At room temperature, methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate is a liquid. It remains stable under normal atmospheric conditions and is typically used in a liquid form within chemical and pharmaceutical applications.

Melting point (Celsius)
49.10
Melting point (Kelvin)
322.25
Boiling point (Celsius)
331.40
Boiling point (Kelvin)
604.55
General information
Molecular weight
313.78g/mol
Molar mass
313.7830g/mol
Density
1.1275g/cm3
Appearence

Methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate appears as a colorless to light yellow liquid. It does not have a strong odor and is visually clear, allowing light to pass through without significant scattering.

Comment on solubility

Solubility of Methyl 5-Chloro-2-[2-(Diethylamino)ethoxy]benzoate

Methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate, with the chemical formula C16H20ClN1O3, exhibits unique solubility characteristics that reflect its complex structure. Understanding its solubility is essential for applications in pharmaceuticals and chemical synthesis.

Key Points on Solubility:

  • Solvent Type: This compound is likely to be soluble in organic solvents such as ethanol and dichloromethane due to its hydrophobic aromatic and ether components.
  • Polarity Considerations: The presence of the diethylamino group can enhance solubility in polar solvents, allowing for increased interaction with water molecules.
  • Temperature Effects: Solubility may increase with higher temperatures, which is typical for many organic compounds.
  • Functional Group Influence: The chloro substituent may influence solubility behavior, enhancing interactions with polar solvents.

In summary, methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate shows variable solubility primarily in polar and non-polar organic solvents, making it a versatile compound in chemical applications.

Interesting facts

Interesting Facts about Methyl 5-Chloro-2-[2-(Diethylamino)ethoxy]benzoate

Methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate is a fascinating compound that blends the intricacies of organic chemistry with practical applications. Here are some key insights:

  • Pharmacological Relevance: This compound is notably used in medicinal chemistry. Its structure features both a benzoate moiety and a diethylamino group, which can interact with biological systems and receptors.
  • Versatile Functional Groups: The presence of the Cl atom signifies its potential utility in electrophilic substitution reactions. The diethylamino group enhances its nucleophilicity, making it a valuable asset for synthetic transformations.
  • Application in Drug Development: Compounds with similar structural frameworks are commonly explored for their pharmacological properties. This compound may serve as a lead compound for developing novel medications.
  • Synthesis Pathways: The synthesis of this compound involves intricate reactions that may include the use of Cl-sourced reagents and esterification techniques, thus providing students with insights into organic synthesis methodologies.
  • Research Opportunity: Researchers are continually exploring the implications of compounds like this one in the field of neuropharmacology. Their ability to cross the blood-brain barrier opens the door to studying their potential effects on neurological conditions.

As we dive deeper into the world of organic compounds, methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate exemplifies the intersection of structure and function in chemistry. Its diverse applications in medicinal chemistry make it an exciting subject for both students and professionals alike!

Synonyms
Sch 1300
5014-26-6
BRN 2696912
BENZOIC ACID, 5-CHLORO-2-(2-(DIETHYLAMINO)ETHOXY)-, METHYL ESTER
5-Chloro-2-(2-(diethylamino)ethoxy)benzoic acid methyl ester
DTXSID80198217
DTXCID10120708
methyl 5-chloro-2-[2-(diethylamino)ethoxy]benzoate
SCHEMBL11570896