Exploration of the structure and interactions of 4-(dimethylamino)-3-methylphenyl <i>N</i> -methylcarbamate (Aminocarb)

Aminocarb [4-(dimethylamino)-3-methylphenyl N-methylcarbamate, C<sub>11</sub>H<sub>16</sub>N<sub>2</sub>O<sub>2</sub>], a synthetic pesticide, was crystallized and characterized by single-crystal and powder X-ray diffraction. In the solid state, the molecules have a strong chain N-H...O hydrogen bond with a strength of -29.37 kJ mol<sup>-1</sup> and a short C-H...π contact that build a wave-like three-dimensional structure. The structural stability and intermolecular interaction of Aminocarb were investigated using differential scanning calorimetry (DSC) and density functional theory (DFT). The results show that the compound is chemically stable, and the two dominating interactions are electrostatic and dispersion energies. An electrostatic potential map reveals the binding sites of the molecules for reactivity. The understanding of the structural stability and interactions in Aminocarb provided in this study could be used to design new compounds with improved solubility and bioavailability. The dimethylamino group and the methyl group on the carbamate could be modified with other alkyl groups, which might reduce the Aminocarb toxicity, thereby leading to the development of safe, efficient and cost-effective compounds.

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Journal
Acta Crystallographica Section C Structural Chemistry
Published
2025-05-05
DOI
https://doi.org/10.1107/s205322962500378x
Primary Topic
Phenothiazines and Benzothiazines Synthesis and Activities
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article
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article

Exploration of the structure and interactions of 4-(dimethylamino)-3-methylphenyl N -methylcarbamate (Aminocarb)

A. Lemmerer, Oluwatoyin Akerele
Acta Crystallographica Section C Structural Chemistry
Phenothiazines and Benzothiazines Synthesis and Activities
article

Exploration of the structure and interactions of 4-(dimethylamino)-3-methylphenyl N -methylcarbamate (Aminocarb)

A. Lemmerer, Oluwatoyin Akerele
article en

Abstract

Aminocarb [4-(dimethylamino)-3-methylphenyl N-methylcarbamate, C<sub>11</sub>H<sub>16</sub>N<sub>2</sub>O<sub>2</sub>], a synthetic pesticide, was crystallized and characterized by single-crystal and powder X-ray diffraction. In the solid state, the molecules have a strong chain N-H...O hydrogen bond with a strength of -29.37 kJ mol<sup>-1</sup> and a short C-H...π contact that build a wave-like three-dimensional structure. The structural stability and intermolecular interaction of Aminocarb were investigated using differential scanning calorimetry (DSC) and density functional theory (DFT). The results show that the compound is chemically stable, and the two dominating interactions are electrostatic and dispersion energies. An electrostatic potential map reveals the binding sites of the molecules for reactivity. The understanding of the structural stability and interactions in Aminocarb provided in this study could be used to design new compounds with improved solubility and bioavailability. The dimethylamino group and the methyl group on the carbamate could be modified with other alkyl groups, which might reduce the Aminocarb toxicity, thereby leading to the development of safe, efficient and cost-effective compounds.

Acta Crystallographica Section C Structural ChemistryVol. 81(6)
University of the Witwatersrand (ZA)
Openalex Percentile: Top 91%
Phenothiazines and Benzothiazines Synthesis and Activities
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