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Relevant bibliographies by topics / 2-aminobenzoic acid

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Academic literature on the topic '2-aminobenzoic acid'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "2-aminobenzoic acid"

1

Lynch, Daniel E., Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "Molecular Cocrystals of Carboxylic Acids. XXVI Adducts of the Amino-Substituted Benzoic Acids with Nitroaromatic Lewis Bases: the Influence of Associative Polyfunctional Substituents on Self-Assembly of Molecules in Cocrystallization Processes." Australian Journal of Chemistry 50, no. 10 (1997): 977. http://dx.doi.org/10.1071/c97067.

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A series of molecular adducts of the isomeric aminobenzoic acids with the nitro-substituted Lewis bases 2-chloro-5-nitropyridine, 5-nitroquinoline and 5-nitroisoquinoline has been prepared and characterized by using infrared spectroscopy and X-ray powder diffraction, and in four cases by single-crystal X-ray diffraction methods. These four compounds are the adducts of 3-aminobenzoic acid with 5-nitroquinoline [(C7H7NO2)(C9H6N2O2)], 4-aminobenzoic acid with 5-nitroquinoline [(C7H7NO2)2(C9H6N2O2)], 2-aminobenzoic acid with 5-nitroisoquinoline [(C7H7NO2)(C9H6N2O2)] and 4-aminobenzoic acid with 5-

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2

Novoa de Armas, Héctor, Oswald M. Peeters, Norbert M. Blaton, Camiel J. De Ranter, and Lisbet Xuárez Marill. "2-(4-Methoxyphenyl)aminobenzoic acid." Acta Crystallographica Section E Structure Reports Online 57, no. 7 (2001): o638—o639. http://dx.doi.org/10.1107/s1600536801010364.

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Jebas, Samuel Robinson, and Thailampillai Balasubramanian. "4-Aminobenzoic acid–nicotinic acid (2/1)." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5621—o5622. http://dx.doi.org/10.1107/s1600536806046812.

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4

Smith, G., JM Gentner, DE Lynch, KA Byriel, and CHL Kennard. "Molecular Cocrystals of Carboxylic Acids. XXI. The Role of Secondary Group Interactions in Adduct Formation Between 2-Aminopyrimidine and Substituted Benzoic Acids: the Crystal Structures of the Adducts With o-Phthalic Acid, o-Nitrobenzoic Acid, o-Aminobenzoic Acid and m-Aminobenzoic Acid." Australian Journal of Chemistry 48, no. 6 (1995): 1151. http://dx.doi.org/10.1071/ch9951151.

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The crystalline adducts of 2-aminopyrimidine (2-ap) with a series of mainly ortho-substituted benzoic acids, o-phthalic acid ( opht ) [(2-ap)( opht )] (1), 2-nitrobenzoic acid (2-nba) [(2-ap)(2-bna)2] (2), 2-aminobenzoic acid (2-aba) [(2-aba) [(2-ap)(2-aba)2] (3) and 3-aminobenzoic acid (3-aba) [(2-ap)(3-aba)] (4) have been prepared and their hydrogen-bonding motifs characterized by using single-crystal X-ray diffraction. The role of substituent groups in secondary associations with cocrystal formation is considered for the 2-aminopyrimidine system.

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5

Kořínková, Jaroslava, Antonín Lyčka, Aleš Cee, Milan Nádvorník, Robert Jirásko, and Radim Hrdina. "Structure of 2:1 cobalt(III) complexes derived from arylazocitrazinic acid." Collection of Czechoslovak Chemical Communications 74, no. 4 (2009): 535–44. http://dx.doi.org/10.1135/cccc2008192.

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1H, 13C NMR and MS spectra of the 2:1 cobalt(III) complexes, the azo coupling products of 2-aminophenol or 2-aminobenzoic acid with the citrazinic acid, were measured and analysed. It was found that the cobalt atom is six-coordinated being bound to two oxygens (one from primary and one from secondary component) and the nitrogen of 2-aminophenol or 2-aminobenzoic acid. Molar magnetic susceptibility data proved the presence of Co(III). Diazotisation of 2-aminophenol or 2-aminobenzoic acid and subsequent coupling reaction with citrazinic acid and complexation of the formed azo product proceeded o

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6

Arman, Hadi D., and Edward R. T. Tiekink. "2-Aminobenzoic acid–4,4′-bipyridine (2/1)." Acta Crystallographica Section E Structure Reports Online 69, no. 9 (2013): o1447. http://dx.doi.org/10.1107/s160053681302271x.

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7

LU, Tian-Huey, Papitra CHATTOPADHYAY, Fen-Ling LIAO, and Jem-Mau LO. "Crystal Structure of 2-Aminobenzoic Acid." Analytical Sciences 17, no. 7 (2001): 905–6. http://dx.doi.org/10.2116/analsci.17.905.

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8

Lynch, Daniel E., Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "Molecular Cocrystals of Carboxylic Acids. XXXII The Crystal Structures of the Adducts of 2-Aminobenzothiazole with 3,5-Dinitrobenzoic Acid (Adduct Hydrate) and 3-Aminobenzoic Acid, and 2-Amino-2-thiazoline with 2-Aminobenzoic Acid." Australian Journal of Chemistry 51, no. 7 (1998): 587. http://dx.doi.org/10.1071/c97204.

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Two adducts of 2-aminobenzothiazole and one of 2-amino-2-thiazoline with aromatic carboxylic acids have been synthesized and their X-ray crystal structures determined. These are 2-aminobenzothiazole with 3,5-dinitrobenzoic acid (the 1 : 1 adduct hydrate) (1), and 3-aminobenzoic acid (1 : 1) (2), and 2-amino-2-thiazoline with 2-aminobenzoic acid (1 : 1) (3). Compound (1) is a non-centrosymmetric proton-transfer complex and gave a signal of 0·30 relative to urea when tested for second-order non-linear optical properties. Compound (3) is also a proton-transfer complex but (2) is not.

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9

Smith, G., DE Lynch, KA Byriel, and CHL Kennard. "Molecular Cocrystals of Carboxylic Acids. XX. The Crystal Structures of 3,5-Dinitrosalicylic Acid and Its Adducts With the Isomeric Monoaminobenzoic Acids." Australian Journal of Chemistry 48, no. 6 (1995): 1133. http://dx.doi.org/10.1071/ch9951133.

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The crystal structure of 3,5-dinitrosalicylic acid monohydrate (1) and its adducts with 2- aminobenzoic acid (2-aba) [( dnsa )(2-aba)] (2), 3-aminobenzoic acid (3-aba) [( dnsa )(3-aba)] (3), and 4-aminobenzoic acid (4-aba) [( dnsa )(4-aba)2] (4), have been determined and the hydrogen bonding associations in each analysed . The acid (1), which is essentially planar, forms strong hydrogen-bonding network associations involving the carboxylic, nitro and phenolic oxygens as well as the lattice water. In all adducts, protonation of the amino group of the second acid occurs, with subsequent hydrogen

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10

Blanksma, J. J., and D. Hoegen. "The sweet taste of 4-nitro-2-aminotoluene, 4-nitro-2-aminobenzoic acid and 2-nitro-4-aminobenzoic acid." Recueil des Travaux Chimiques des Pays-Bas 65, no. 5 (2010): 333–37. http://dx.doi.org/10.1002/recl.19460650504.

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Book chapters on the topic "2-aminobenzoic acid"

1

Abo, Mitsuru, Li-ping He, Kae Sato, and Akira Okubo. "Determination of Monosaccharides Derivatized with 2-Aminobenzoic Acid by Capillary Electrophoresis." In Capillary Electrophoresis of Biomolecules. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-296-4_4.

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2

Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) complex with Schiff-base derived from 4-aminoantipyrine and 2-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_127.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with Schiff-base derived from 4-aminoantipyrine and 2-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_208.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) complex with Schiff-base derived from 4-aminoantipyrine and 2-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_59.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base derived from 4-aminoantipyrine and 2-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_387.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with Schiff-base derived from 4-aminoantipyrine and 2-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_282.

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7

Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadyl complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_87.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mononuclear cobalt(II) complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_482.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mononuclear nickel(II) complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_176.

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10

Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_475.

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Conference papers on the topic "2-aminobenzoic acid"

1

Zavtoni, Pantelimon, Aurelia Stingaci, Anna Samoilova, Violetta Goncharuk, Maria Lisouskaya, and Al Mihalichiuk. "Eficacitatea tratării plantelor la cartof cu suspensii de bacterii entomopatogene în sinergie cu derivați ai acidului para-aminobenzoic." In Scientific International Symposium "Plant Protection – Achievements and Perspectives". Institute of Genetics, Physiology and Plant Protection, Republic of Moldova, 2023. http://dx.doi.org/10.53040/ppap2023.36.

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Researchers from the Republic of Moldova jointly with those from the Republic of Belarus have conducted studies on the growing conditions in 2022 for the "Riviera" potato variety, assessing the influence of the consequences of unfavorable climatic factors on the formation of the photosynthetic potential and productivity of plants, the quantity and quality of the harvest. Thus, after the second decade of May 2022, at the USM's IGFPP potato lot, experiments were mounted according to the scheme: treatment with para-aminobenzoic acid (PABA) derivatives 10-2,10-4, 10-6 in complex with Bacillus thur

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2

Stingaci, Aurelia, and Violetta Goncharuk. "Strategii eco cu produse biologice în livezile de mar." In VIIIth International Scientific Conference “Genetics, Physiology and Plant Breeding”. Institute of Genetics, Physiology and Plant Protection, 2024. https://doi.org/10.53040/gppb8.2024.128.

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Products of microbial origin in combined with para-aminobenzoic acid (pABA) derivatives, can be the basis for organic farming and plant resistance to unfavorable environmental factors inducing, as well as for the crop yield increase. The article presents the results of the study of the efficiency of fruit-cultures and potato plantations treatment with aqueous suspensions of entomopathogenic bacteria Bacillus thuringiensis subsp. kurstaki and Bacillus thuringiensis var. thuringiensis with addition of para-aminobenzoic acid derivatives solutions in concentrations 10-2, 10-4, 10-6 mM.. The result

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3

Stingaci, Aurelia, Pantelimon Zavtoni, Tatiana Scerbacova, et al. "Studiu eficacității complexe al agenților biologici la măr și cartof la temperaturi ridicate." In Scientific International Symposium "Plant Protection – Achievements and Perspectives". Institute of Genetics, Physiology and Plant Protection, Republic of Moldova, 2023. http://dx.doi.org/10.53040/ppap2023.33.

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Products of microbial origin in combination with para-aminobenzoic acid (PABA) derivatives, can be the basis for organic farming and plant resistance to unfavorable environmental factors inducing, as well as for the crop yield increasing. The article presents the results of the study of efficiency of fruit-cultures and potato plantations treatment with aqueous suspensions of entomopathogenic bacteria Bacillus thuringiensis subsp. kurstaki and Bacillus thuringiensis var. thuringiensis with addition of para-aminobenzoic acid derivatives solutions in concentrations 10-2, 10-4, 10-6 mol/l. An incr

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4

ARSENE, Ion, and Viorica PURCEL. "Studiul DFT a descriptorilor de reactivitate pentru acizii o-, m- și p-aminobenzoic." In "Învățământul superior: tradiţii, valori, perspective", conferinţă ştiinţifică internaţională. Ion Creangă Pedagogical State University, 2022. https://doi.org/10.46727/c.v1.1-2-10-2022.p42-49.

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Theoretical DFT calculations were used for the study of o-, m- and p-aminobenzoic acids, optimizing the geometric structures, and determining the thermodynamic stability of the studied compounds. The value of the variation for the frontier HOMO-LUMO orbitals both in the gas phase and in the solvent gives the possibility to determine some reactivity descriptors. Calculating the energy and stability descriptors of the studied conformers shows a close correlation. Also, following the investigations, it can be concluded that the most stable isomer of the studied amino acid is o-aminobenzoic acid,

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