Molecular structure of 4-Bromoaniline, CAS Number: 106-40-1
4-Bromoaniline (CAS 106-40-1)
Alternate Names:
p-Bromophenylamine
Application:
4-Bromoaniline is a brominated aniline used as a building block
CAS Number:
106-40-1
Molecular Weight:
172.02
Molecular Formula:
C6H6BrN
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
4-Bromoaniline is a chemical compound that functions as a building block in organic synthesis. It acts as a precursor in the production of various dyes, and agrochemicals. Its mechanism of action involves participating in nucleophilic aromatic substitution reactions, where the bromine atom is substituted with other functional groups to create new compounds. 4-Bromoaniline plays a role in the modification of aromatic compounds, allowing for the introduction of specific functional groups at the para position. In experimental applications, 4-Bromoaniline is utilized to facilitate the synthesis of complex organic molecules by serving as a starting material for the construction of diverse chemical structures. Its molecular properties enable it to undergo various chemical transformations, making it a versatile component in the development of novel compounds.
4-Bromoaniline (CAS 106-40-1) References
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- Identification of the urinary metabolites of 4-bromoaniline and 4-bromo-[carbonyl-13C]-acetanilide in rat. | Scarfe, GB., et al. 2002. Xenobiotica. 32: 325-37. PMID: 12028665
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- Proton-transfer compounds of 8-hydroxy-7-iodoquinoline-5-sulfonic acid (ferron) with 4-chloroaniline and 4-bromoaniline. | Smith, G., et al. 2007. Acta Crystallogr C. 63: o405-7. PMID: 17609572
- Mechanism of inhibition of myeloperoxidase by anti-inflammatory drugs. | Kettle, AJ. and Winterbourn, CC. 1991. Biochem Pharmacol. 41: 1485-92. PMID: 1850278
- The metabolism of 4-bromoaniline in the bile-cannulated rat: application of ICPMS ((79/81)Br), HPLC-ICPMS & HPLC-oaTOFMS. | Duckett, C., et al. 2015. Xenobiotica. 45: 672-80. PMID: 25837688
- Studies on Oligomer Metal Complexes Derived from Bisamic Acid of Pyromellitic Dianhydride and 4-Bromoaniline. | Patel, YS. 2014. Int Sch Res Notices. 2014: 516274. PMID: 27379295
- N-([1,1'-biaryl]-4-yl)-1-naphthamide-based scaffolds synthesis, their cheminformatics analyses, and screening as bacterial biofilm inhibitor. | Ejaz, S., et al. 2022. J Basic Microbiol. 62: 1143-1155. PMID: 34724237
- Bright Luminescent Carbon Dots for Multifunctional Selective Sensing and Imaging Applications in Living Cells. | Thirumalaivasan, N. and Wu, SP. 2020. ACS Appl Bio Mater. 3: 6439-6446. PMID: 35021775
- Synthesis of Functionalized N-(4-Bromophenyl)furan-2-carboxamides via Suzuki-Miyaura Cross-Coupling: Anti-Bacterial Activities against Clinically Isolated Drug Resistant A. baumannii, K. pneumoniae, E. cloacae and MRSA and Its Validation via a Computational Approach. | Siddiqa, A., et al. 2022. Pharmaceuticals (Basel). 15: PMID: 35890140
- Microbial mineralization of ring-substituted anilines through an ortho-cleavage pathway. | Zeyer, J., et al. 1985. Appl Environ Microbiol. 50: 447-53. PMID: 4051488
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Bromoaniline, 5 g | sc-256720 | 5 g | $17.00 | |||
4-Bromoaniline, 100 g | sc-256720A | 100 g | $65.00 |