Relevant bibliographies by topics / 4-Bromoaniline

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Academic literature on the topic '4-Bromoaniline'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "4-Bromoaniline"

1

Khalaji, Aliakbar Dehno, Alexandra M. Z. Slawin, and J. Derek Woollins. "N-(2-Benzylidenepropylidene)-4-bromoaniline." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4257. http://dx.doi.org/10.1107/s1600536807048222.

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The title compound, C16H14BrN, at 93 (2) K crystallizes with two independent molecules in the asymmetric unit. The molecules are slightly non-planar with the substituents adopting an E configuration with respect to the imine C=N bond.
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2

Ran, deep Kaur Sandhar, R. Sharma J., and R. Manrao M. "Synthesis and fungitoxicity of aldimines and 4-thiazolidinones derived from 4-bromoaniline." Journal of Indian Chemical Society Vol. 85, Feb 2008 (2008): 220–23. https://doi.org/10.5281/zenodo.5808967.

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Department of Biochemistry and Chemistry, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>Manuscript received 26 October 2005, revised 1 August 2007, accepted 26 November 2007</em> Condensation of 4-bromoaniline with benzaldehyde and substituted benzaldehydes (1-8) in equimolar ratio resulted in the formation of benzal-4-bromoaniline and its C-phenyl derivatives (la-8a). Addition of thioglycolic acid to la-8a yielded the respective 4-thiazolidinone (lb-8b). The synthesized compounds were characterized on the basis of elemental analysis and spectral studies and were screened
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3

Harikishna, V., and N. V. S. Naidu. "Facile and Sensitive Spectrophotometric Technique for the Determination of Carbofuran in its Formulations, Water and Grain Samples with Substituted Anilines." E-Journal of Chemistry 2, no. 4 (2005): 218–23. http://dx.doi.org/10.1155/2005/172909.

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Methods are described for the determination of carbofuran in its formulations, in water and grain samples by the diazotization coupling spectrophotometric technique, using substituted anilines such as 4-bromoaniline, 4-methylaniline and 4-aminobenzaldehyde as the coupling agents. The orange red colour formed with 4-bromoaniline shows maximum absorption at 478 nm, yellow colour obtained with 4-methylaniline have maximum absorption at 465 nm whereas a red colour derivative formed with 4-aminobenzaldehyde shows λmaxat 472 nm. The methods could be successfully applied for the determination of carb
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4

KHALAJI, Aliakbar Dehno, та William T. A. HARRISON. "Crystal Structure of β-Phenylcinnamaldehyde-4-bromoaniline". Analytical Sciences: X-ray Structure Analysis Online 24 (2008): x3—x4. http://dx.doi.org/10.2116/analscix.24.x3.

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5

Xie, Yu, Xiao-Wei Hong, and Ya Wei. "Crystal structure of N-diphenylphosphoryl-4-bromoaniline, C18H15BrNOP." Zeitschrift für Kristallographie - New Crystal Structures 225, no. 2 (2010): 349–50. http://dx.doi.org/10.1524/ncrs.2010.0152.

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6

Delaporte, Nicolas, Karim Zaghib, and Daniel Bélanger. "In situ formation of bromobenzene diazonium ions and their spontaneous reaction with carbon-coated LiFePO4 in organic media." New Journal of Chemistry 40, no. 7 (2016): 6135–40. http://dx.doi.org/10.1039/c6nj00132g.

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7

Mishra, Manish Kumar, Pallavi Ghalsasi, M. N. Deo, et al. "In situhigh pressure study of an elastic crystal by FTIR spectroscopy." CrystEngComm 19, no. 47 (2017): 7083–87. http://dx.doi.org/10.1039/c7ce01664f.

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Anin situhigh pressure-FTIR study on a 2,3-dichlorobenzylidine-4-bromoaniline elastic crystal shows significant structural changes at high pressure which revert back to the ambient structure on decompression.
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8

Gao, Wei. "Synthesis and Structure Analysis of N-diphenylphosphoryl-4-bromoaniline." Molecular Crystals and Liquid Crystals 609, no. 1 (2015): 155–60. http://dx.doi.org/10.1080/15421406.2014.950469.

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9

Bei, M. P., and A. P. Yuvchenko. "Synthesis of aromatic and heterocyclic fumaropimaric acid triamides." Журнал общей химии 93, no. 7 (2023): 1001–6. http://dx.doi.org/10.31857/s0044460x2307003x.

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A method was developed for the synthesis of previously unknown triamides of fumaropimaric acid by the reaction of anilide and 1-(piperidin-1-ylcarbonyl) derivative of fumaropimaric acid with aromatic and heterocyclic amines [4-toluidine, 4-pentylaniline, 4-biphenylamine, 4-methoxy-, ethoxy-, phenoxy-, bromoaniline, 2-picolylamine, 2-(aminomethyl)furan, 2-(aminomethyl)thiophene] under the action of propanephosphonic acid anhydride.
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10

Johmoto, Kohei, Takashi Ishida, Akiko Sekine, Hidehiro Uekusa, and Yuji Ohashi. "Relation between photochromic properties and molecular structures in salicylideneaniline crystals." Acta Crystallographica Section B Structural Science 68, no. 3 (2012): 297–304. http://dx.doi.org/10.1107/s0108768112010993.

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The crystal structures of the salicylideneaniline derivatives N-salicylidene-4-tert-butyl-aniline (1), N-3,5-di-tert-butyl-salicylidene-3-methoxyaniline (2), N-3,5-di-tert-butyl-salicylidene-3-bromoaniline (3), N-3,5-di-tert-butyl-salicylidene-3-chloroaniline (4), N-3,5-di-tert-butyl-salicylidene-4-bromoaniline (5), N-3,5-di-tert-butyl-salicylidene-aniline (6), N-3,5-di-tert-butyl-salicylidene-4-carboxyaniline (7) and N-salicylidene-2-chloroaniline (8) were analyzed by X-ray diffraction analysis at ambient temperature to investigate the relationship between their photochromic properties and mo
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Book chapters on the topic "4-Bromoaniline"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base (derived from 2,6-diformyl-4-methylphenol and 4-bromoaniline)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_422.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base (derived from 2,6-diformyl-4-t-butylphenol and 4-bromoaniline)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_424.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with Schiff base derived from thiophene-2-aldehyde and 4-bromoaniline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_548.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base derived from thiophene-2-aldehyde and 4-bromoaniline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_236.

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5

Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand copper(II) complex with Schiff-base (derived from 2,6-diformyl-4-methylphenol and 4-bromoaniline) and 2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_423.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand copper(II) complex with Schiff-base (derived from 2,6-diformyl-4-methylphenol and 4-bromoaniline) and 2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_425.

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You might also be interested in the extended bibliographies on the topic '4-Bromoaniline' for particular source types:
Journal articles
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