Date published: 2025-10-17

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3-Bromo-4-methoxyphenethylamine (CAS 159465-27-7)

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CAS Number:
159465-27-7
Molecular Weight:
230.10
Molecular Formula:
BrC6H3(OCH3)(CH2CH2NH2)
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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3-Bromo-4-methoxyphenethylamine is a compound that functions as a substrate in the synthesis of various organic compounds. It acts as a precursor in the formation of complex molecules through chemical reactions, contributing to the development of novel materials and substances. At the molecular level, 3-Bromo-4-methoxyphenethylamine undergoes specific transformations and interactions with other reagents, leading to the creation of diverse chemical structures. Its mechanism of action involves participating in substitution, addition, or condensation reactions, enabling the production of derivatives with distinct properties. 3-Bromo-4-Methoxyphenethylamine plays a role in the modification of molecular frameworks, serving as a building block for the construction of advanced chemical entities. Its involvement in processes contributes to the exploration of new chemical pathways and the generation of diverse molecular architectures.


3-Bromo-4-methoxyphenethylamine (CAS 159465-27-7) References

  1. Total synthesis and biological evaluation of the marine bromopyrrole alkaloid dispyrin: elucidation of discrete molecular targets with therapeutic potential.  |  Kennedy, JP., et al. 2008. J Nat Prod. 71: 1783-6. PMID: 18800848
  2. Synthetic analogs of stryphnusin isolated from the marine sponge Stryphnus fortis inhibit acetylcholinesterase with no effect on muscle function or neuromuscular transmission.  |  Moodie, LW., et al. 2016. Org Biomol Chem. 14: 11220-11229. PMID: 27841892
  3. Identification of Quorum Sensing Activators and Inhibitors in The Marine Sponge Sarcotragus spinosulus.  |  Saurav, K., et al. 2020. Mar Drugs. 18: PMID: 32093216
  4. Construction of N-Heterocycles Fused with a Highly Substituted Benzene Ring by a Benzyne-Mediated Cyclization/Functionalization Cascade Reaction and Its Application to the Total Synthesis of Marine Natural Products.  |  Tokuyama, H. 2021. Chem Pharm Bull (Tokyo). 69: 707-716. PMID: 34334514
  5. Inhibition of the Quorum Sensing System, Elastase Production and Biofilm Formation in Pseudomonas aeruginosa by Psammaplin A and Bisaprasin.  |  Oluwabusola, ET., et al. 2022. Molecules. 27: PMID: 35268822
  6. Synthesis and molecular modeling of 1-phenyl-1,2,3,4-tetrahydroisoquinolines and related 5,6,8,9-tetrahydro-13bH-dibenzo[a,h]quinolizines as D1 dopamine antagonists.  |  Minor, DL., et al. 1994. J Med Chem. 37: 4317-28. PMID: 7996543

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3-Bromo-4-methoxyphenethylamine, 1 g

sc-225968
1 g
$57.00