Relevant bibliographies by topics / N-Methylphenyl thiourea

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Academic literature on the topic 'N-Methylphenyl thiourea'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "N-Methylphenyl thiourea"

1

Zhang, Bin, Bi-Quan Su, and Liang Xian. "N-Benzoyl-N′-(2-methylphenyl)thiourea." Acta Crystallographica Section E Structure Reports Online 62, no. 9 (2006): o4024—o4026. http://dx.doi.org/10.1107/s1600536806032740.

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2

Lin, Qi, You-Ming Zhang, Tai-bao Wei, and Hai Wang. "N-Ethoxycarbonyl-N′-(2-methylphenyl)thiourea." Acta Crystallographica Section E Structure Reports Online 60, no. 4 (2004): o580—o582. http://dx.doi.org/10.1107/s1600536804005161.

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3

Yusof, M. Sukeri M., A. Sahali Mardi, and Bohari M. Yamin. "N-(4-Methoxybenzoyl)-N′-(4-methylphenyl)thiourea." Acta Crystallographica Section E Structure Reports Online 61, no. 10 (2005): o3357—o3358. http://dx.doi.org/10.1107/s1600536805029478.

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4

Razis, S. Aminah A., M. Sukeri M. Yusof, A. Maisara Kadir, and Bohari M. Yamin. "N-(4-Methylbenzoyl)-N′-(4-methylphenyl)thiourea." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4395. http://dx.doi.org/10.1107/s1600536807049720.

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The title compound, C16H16N2OS, adopts a trans–cis configuration of the 4-methylbenzoyl and 4-methylphenyl groups, with respect to the thiono S atom across the thiourea C—N bonds. The dihedral angle between the two groups is 10.36 (8)°. The structure is stabilized by intermolecular hydrogen bonds which form dimers. There are also intramolecular hydrogen bonds.
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5

Xian, Liang. "N-(3-Methylphenyl)-N′-(4-nitrobenzoyl)thiourea." Acta Crystallographica Section E Structure Reports Online 64, no. 10 (2008): o1969. http://dx.doi.org/10.1107/s1600536808029425.

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6

Semwal, Amit, Amit Nigam, and D. C. P. Singh. "Synthesis, Characterization and Biological Activity of Novel N-p-methylbenzoyl-N’ substituted thiourea." International Journal of Drug Design and Discovery 2, no. 4 (2011): 654–58. https://doi.org/10.37285/ijddd.2.4.7.

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A series of N-p-methylbenzoyl-N’ thiourea derivatives bearing different substituents have been synthesized and screened in order to evaluate for their antibacterial and antifungal activity. Antibacterial and antifungal activity of the title compounds has been evaluated by varying the substituents in the thiourea moiety. Reaction of p-methylbenzoyl chloride with ammonium thiocynate followed by the addition of various aromatic amines afforded N-p-methylbenzoyl-N’ substituted thiourea. The structures of newly synthesized compounds has been supported by IR and 1HNMR spectral analysis. Among the sy
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7

Zhang, You-Ming, Liang Xian та Tai-Bao Wei. "Chlorobis[N′-ethoxycarbonyl-N-(4-methylphenyl)thiourea-κS]copper(I)". Acta Crystallographica Section C Crystal Structure Communications 59, № 11 (2003): m473—m474. http://dx.doi.org/10.1107/s0108270103022285.

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The title complex, chlorobis{ethyl N-[(4-methylanilino)thiocarbonyl]carbamate-κS}copper(I), [CuCl(C11H14N2O2S)2], was synthesized by the reaction of cupric chloride with the corresponding thiourea derivative. The complex has imposed crystallographic m symmetry and the CuI coordination environment is trigonal planar, formed by two S atoms and one Cl atom. The formation of intramolecular hydrogen bonds promotes the stability of the complex.
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8

Yeo, Chien, and Edward Tiekink. "1-[N-Methyl-N-(Phenyl)amino]-3- (4-Methylphenyl)Thiourea." Molbank 2019, no. 1 (2019): M1052. http://dx.doi.org/10.3390/m1052.

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The title compound, 1-[N-methyl-N-(phenyl)amino]-3-(4-methylphenyl)thiourea (1), was synthesized by the reaction of 1-methyl-1-phenyl hydrazine and 4-tolyl isothiocyanate, and was characterized by spectroscopy (1H and 13C{1H} NMR, IR, and UV), elemental analysis as well as by single crystal X-ray crystallography. In the solid state, the molecule exists as the thioamide tautomer and features an anti-disposition of the thioamide–N–H atoms; an intramolecular N–H⋯N hydrogen bond is noted. The molecular conformation resembles that of the letter L. In the molecular packing, thioamide-N1–H⋯S1(thione)
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9

Dolzhenko, Anton V., Geok Kheng Tan, Lip Lin Koh, Anna V. Dolzhenko, and Wai Keung Chui. "N-Carbethoxy-N′-[3-(4-methylphenyl)-1H-1,2,4-triazol-5-yl]thiourea." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (2010): o549—o550. http://dx.doi.org/10.1107/s1600536810004289.

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10

Du, Hai-Tang, Ming Lu, Wei-Yi Zhou, and Li-Li Sun. "N-(5-Chloro-3-methyl-1-phenylpyrazol-4-ylcarbonyl)-N′-(4-methylphenyl)thiourea." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4287. http://dx.doi.org/10.1107/s1600536807043541.

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The crystal structure of the title compound, C19H17ClN4OS, has been determined in order to elucidate the molecular conformation. The pyrazole ring makes dihedral angles of 74.3 (3)° and 2.9 (3)° with the phenyl and tolyl rings, respectively; these two six-membered rings are twisted by 71.6 (3)° with respect to each other. The crystal packing of the title compound is stabilized by intramolcular N—H...O and intermolcular N—H...S hydrogen bonds.
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Book chapters on the topic "N-Methylphenyl thiourea"

1

Amose, Yardily, Fathima Shahana, and Abbs Fen Reji. "Density Functional Theory and Molecular Modeling of the Compound 2-[2-(4-Methylphenylamino)-4-phenylthiazol-5-yl]benzofuran." In Furan Derivatives - Recent Advances and Applications. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.99577.

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The compound 2-[2-(4-methylphenylamino)-4-phenylthiazol-5-yl]benzofuran was prepared from 1-(4-methylphenyl)-3-(N-phenylbenzimidoyl)thiourea and 2-(2-bromoacetyl) benzofuran in the presence of triethylamine and characterized by FTIR, NMR, and mass spectra. Density functional theory (DFT) computations were adopted for the geometry optimization of this compound, to evaluate their Mulliken atomic charge distribution, HOMO-LUMO energy gap, and vibrational analysis. The titled compound induced G1 cell cycle arrest, which is regulated by CDK2 in cancer cells. Therefore, we used molecular modeling to
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