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Preparation and In Vivo Use of an Activity-based Probe for N-acylethanolamine Acid Amidase
Published on: November 23, 2016
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4-[(2-Phenyl-eth-yl)amino]-benzoic acid.
1School of Chemical Engineering and Pharmacy Wuhan Institute of Technology,Wuhan Hubei 430205 People's Republic of China.
Iucrdata
|September 9, 2024
Summary
This study reveals that the title compound (C15H15NO2) forms an acid-acid dimer in its crystalline structure. This dimerization occurs through specific hydrogen bonds between the molecules.
Area of Science:
- Crystallography
- Supramolecular Chemistry
- Organic Chemistry
Background:
- Understanding molecular interactions in the solid state is crucial for materials science.
- Hydrogen bonding plays a key role in the self-assembly of organic molecules.
- Crystal structure analysis provides insights into intermolecular forces.
Purpose of the Study:
- To determine the crystal structure of the title compound (C15H15NO2).
- To investigate the intermolecular interactions governing the compound's solid-state arrangement.
- To characterize the formation of supramolecular structures in the crystal.
Main Methods:
- Single-crystal X-ray diffraction was employed to analyze the crystal structure.
- The crystallographic data were processed to determine the unit cell parameters and atomic positions.
- Hydrogen bonding networks were identified and analyzed.
Main Results:
- The title compound, C15H15NO2, crystallizes with two molecules in the asymmetric unit.
- The two molecules in the asymmetric unit associate to form a distinct acid-acid dimer.
- Pairwise O-H⋯O hydrogen bonds are responsible for the observed dimer formation.
Conclusions:
- The crystal structure of C15H15NO2 is characterized by the formation of acid-acid dimers.
- Hydrogen bonding is the primary driving force for this self-assembly in the solid state.
- The findings contribute to the understanding of supramolecular chemistry and crystal engineering.
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