Date published: 2026-4-30

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2′,4′,6′-Trimethoxyacetophenone (CAS 832-58-6)

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CAS Number:
832-58-6
Molecular Weight:
210.23
Molecular Formula:
C11H14O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,4,6-Trimethoxyacetophenone, known as TMAP, is a synthetic aromatic compound that finds widespread applications in the field of chemistry. 2,4,6-Trimethoxyacetophenone (TMAP) has proven to be invaluable in numerous scientific research applications. The primary use of 2,4,6-Trimethoxyacetophenone lies in its capacity as a starting material for organic compound synthesis. Acting as a nucleophile, it readily reacts with electrophiles to engender the formation of novel compounds. Generally, these reactions manifest as substitution reactions, wherein an atom or group of atoms is substituted by another atom or group of atoms.


2′,4′,6′-Trimethoxyacetophenone (CAS 832-58-6) References

  1. A novel chalcone derivative which acts as a microtubule depolymerising agent and an inhibitor of P-gp and BCRP in in-vitro and in-vivo glioblastoma models.  |  Boumendjel, A., et al. 2009. BMC Cancer. 9: 242. PMID: 19619277
  2. Synthesis and biological evaluation of isomeric methoxy substitutions on anti-cancer indolyl-pyridinyl-propenones: Effects on potency and mode of activity.  |  Trabbic, CJ., et al. 2016. Eur J Med Chem. 122: 79-91. PMID: 27343855
  3. Polymeric glabrescione B nanocapsules for passive targeting of Hedgehog-dependent tumor therapy in vitro.  |  Ingallina, C., et al. 2017. Nanomedicine (Lond). 12: 711-728. PMID: 28322108
  4. A comprehensive review of the ethnomedicine, phytochemistry, pharmacological activities of the genus Kniphofia.  |  Nigussie, G., et al. 2022. Pharm Biol. 60: 1177-1189. PMID: 35701101

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2′,4′,6′-Trimethoxyacetophenone, 5 g

sc-254393
5 g
$54.00