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Ethyl 2-(N-benzoyl-3,4-dichloroanilino)propanoate

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Identification
Molecular formula
C18H17Cl2NO3
CAS number
3546-36-9
IUPAC name
ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate
State
State

At room temperature, ethyl 2-(N-benzoyl-3,4-dichloroanilino)propanoate exists as a solid. The crystalline structure is stable under normal conditions.

Melting point (Celsius)
112.00
Melting point (Kelvin)
385.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
366.24g/mol
Molar mass
366.1990g/mol
Density
1.4000g/cm3
Appearence

Ethyl 2-(N-benzoyl-3,4-dichloroanilino)propanoate is typically a crystalline solid. The color can vary but often appears as off-white to pale yellow, possibly due to impurities or specific synthesis routes used.

Comment on solubility

Solubility of Ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate

Ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate is a unique compound with intriguing solubility characteristics. Understanding its solubility is essential, as it can greatly influence its applications in various fields such as pharmaceuticals, agrochemicals, and materials science. Here are some key points regarding its solubility:

  • Solvent Types: This compound is expected to exhibit varying solubility in polar and non-polar solvents. It may demonstrate higher solubility in organic solvents like ethanol and acetone due to its hydrophobic aromatic rings.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, making it more soluble in warm solvents compared to cold.
  • pH Influence: The solubility can also be significantly affected by the pH of the solution, owing to potential ionization of functional groups under varying pH conditions.
  • Potential Applications: Its unique solubility properties can be harnessed for selective synthesis or extraction processes, particularly in organic synthesis.

In conclusion, while specific solubility data may require experimental determination, these general considerations highlight the importance of solvent choice, temperature, and pH in establishing the solubility profile of ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate.

Interesting facts

Interesting Facts about Ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate

Ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate is a fascinating compound that showcases the intricate world of synthetic organic chemistry. This compound, primarily known for its utility in various chemical synthesis applications, stands out due to its unique structure and the properties imparted by its components.

Key Features:

  • Functional Diversity: This compound contains multiple functional groups, including an ester, amine, and carbonyl. This allows for versatile reactivity and the potential for diverse applications in pharmaceuticals and agrochemicals.
  • Role in Synthesis: Ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate is often used as an intermediate in the synthesis of complex organic molecules, illustrating the importance of intermediates in the drug development process.
  • Biological Interest: The presence of the dichloro-aniline moiety suggests a potential for biological activity, which has earned the attention of researchers exploring its effects and efficacy in medicinal chemistry.
  • Collaborative Research: Being a compound with multiple functional groups, it opens up avenues for collaborative research across fields such as medicinal chemistry, environmental science, and material science.

One of the most intriguing aspects of this compound is its incorporation of the 3,4-dichlorophenyl structure, which is often related to compounds with significant biological properties. The presence of chlorines can enhance the lipophilicity of the molecules, potentially affecting the pharmacokinetics of drugs derived from such compounds. Conclusively, Ethyl 2-(N-benzoyl-3,4-dichloro-anilino)propanoate not only represents an important building block in synthetic organic chemistry but also serves as a reminder of the complex interactions between structure and reactivity in chemical compounds.

Synonyms
Benzoylprop-ethyl
22212-55-1
Suffix
Endaven
Alanine, N-benzoyl-N-(3,4-dichlorophenyl)-, ethyl ester
95764D9P7D
DTXSID7040281
FX-2182
Ethyl-2-(N-benzoyl-3,4-dichloroanilino)propionate
RefChem:118812
DTXCID5020281
244-845-5
H04Q4O243C
Karakhol
BENZOYLPROP ETHYL
Suffix 25
Ethyl 2-[benzoyl-(3,4-dichlorophenyl)amino]propanoate
FX 2182
ethyl 2-(N-benzoyl-3,4-dichloroanilino)propanoate
SD 30,053
N-Benzoyl-N-(3,4-dichlorophenyl)-DL-alanine ethyl ester
DL-Alanine, N-benzoyl-N-(3,4-dichlorophenyl)-, ethyl ester
Alanine, N-benzoyl-N-(3,4-dichlorophenyl)-, ethyl ester, DL-
BRN 3007699
Ethyl 2-(N-benzoyl-3,4-dichloroanilino)propionate
Benzoylprop-ethyl [BSI:ISO]
EINECS 244-845-5
Ethyl N-benzoyl-N-(3,4-dichlorophenyl)-DL-alaninate
UNII-95764D9P7D
Ethyl (+-)-2-(N-benzoyl-3,4-dichloroanilino)propionate
Ethyl (+-)-2-(N-(3,4-dichlorophenyl)benzamido)propionate
(+-)-Ethyl N-benzoyl-N-(3,4-dichlorophenyl)-2-aminopropionate
SCHEMBL163055
BENZOYLPROP-ETHYL [ISO]
CHEBI:82171
AKOS015915519
Propionic acid, 2-(N-benzoyl-N-(3,4-dichlorophenyl))amino-, ethyl ester, (+-)-
NS00001839
C19044
A816018
Ethyl 2-(benzoyl-3,4-dichloroanilino)propanoate #
Benzoylprop-ethyl, PESTANAL(R), analytical standard
Ethyl 2-[benzoyl(3,4-dichlorophenyl)amino]propionate
Ethyl 2-[N-(3,4-dichlorophenyl)benzamido]propionate
Q22831374
Ethyl N-benzoyl-N-(3,4-dichlorophenyl)-2-aminopropionate
Propionic acid, 2-(N-benzoyl-N-(3,4-dichlorophenyl))amino-, ethyl ester
Propionic acid, 2-(N-benzoyl-N-(3,4-dichlorophenyl))amino-, ethyl ester, (.+/-.)-