Date published: 2026-7-25

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2,5-Dimethoxybenzylamine (CAS 3275-95-4)

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Alternate Names:
Benzenemethanamine; 1-(2,5-dimethoxyphenyl)methanamine; 2,5-Dimethoxybenzenemethanamine
CAS Number:
3275-95-4
Molecular Weight:
167.21
Molecular Formula:
C9H13NO2
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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2,5-Dimethoxybenzylamine is a derivative of benzylamine, containing two methoxy substituents at the 2 and 5 positions. It is a precursor in the synthesis of various organic compounds, particularly in agrochemical industries. 2,5-Dimethoxybenzylamine has the ability to undergo selective functionalization reactions, making it a useful building block for the preparation of diverse chemical structures. In biochemistry, 2,5-dimethoxybenzylamine is a reagent in the synthesis of biologically active molecules, due to its versatile reactivity and compatibility with a wide range of functional groups. Its unique chemical properties allow for the efficient modification of complex molecular scaffolds, enabling the creation of novel compounds with potential applications in chemical biology. 2,5-dimethoxybenzylamine plays a role in the development of new chemical entities with potential bioactive properties.


2,5-Dimethoxybenzylamine (CAS 3275-95-4) References

  1. N6-benzyladenosine derivatives as novel N-donor ligands of platinum(II) dichlorido complexes.  |  Starha, P., et al. 2013. Molecules. 18: 6990-7003. PMID: 23771060
  2. Bifunctional building blocks in the Ugi-azide condensation reaction: a general strategy toward exploration of new molecular diversity.  |  Gunawan, S. and Hulme, C. 2013. Org Biomol Chem. 11: 6036-46. PMID: 23912086
  3. Benzoquinones as inhibitors of botulinum neurotoxin serotype A.  |  Bremer, PT., et al. 2014. Bioorg Med Chem. 22: 3971-81. PMID: 24984937
  4. Prevalence of toxigenic fungi and mycotoxins in Arabic coffee (Coffea arabica): Protective role of traditional coffee roasting, brewing and bacterial volatiles.  |  Al Attiya, W., et al. 2021. PLoS One. 16: e0259302. PMID: 34714880
  5. Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor-Acceptor Cyclopropanes and Anilines/Benzylamines.  |  Boichenko, MA., et al. 2022. Molecules. 27: PMID: 36500574

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,5-Dimethoxybenzylamine, 5 g

sc-231116
5 g
$65.00