3-Hydroxyacetophenone (Standard)3-Hydroxyacetophenone (Standard) - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-Y0603R.804-HY-Y0603R804-HY-Y0603RBusiness & Industrial > Science & Laboratory3-Hydroxyacetophenone (Standard)
Gentaur
EUR12027-02-24

3-Hydroxyacetophenone (Standard)

CAT:
804-HY-Y0603R
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
3-Hydroxyacetophenone (Standard) - image 1

3-Hydroxyacetophenone (Standard)

  • Description:

    3-Hydroxyacetophenone (Standard) is the analytical standard of 3-Hydroxyacetophenone (HY-Y0603) . This product is intended for research and analytical applications. 3-Hydroxyacetophenone (m-Hydroxyacetophenone) is a hydroxy-substituted alkyl phenyl ketone and also a plant defensin in carnations. 3-Hydroxyacetophenone has antifusarium activity. In addition, 3-Hydroxyacetophenone can be used to synthesize Rivastigmine (HY-17368) [1][2][3].
  • Target:

    Drug Intermediate; Fungal; Reference Standards
  • Related Pathways:

    Anti-infection; Others
  • Field of Research:

    Others
  • Smiles:

    CC(C1=CC=CC(O)=C1)=O
  • Molecular Formula:

    C8H8O2
  • Molecular Weight:

    136.15
  • References & Citations:

    [1]Katharine Moore Tibbetts, et al. Controlling dissociation of alkyl phenyl ketone radical cations in the strong-field regime through hydroxyl substitution position. J Phys Chem A. 2014 Sep 18;118 (37) :8170-6.|[2]Kiwon Han, et al. Chemoenzymatic synthesis of rivastigmine via dynamic kinetic resolution as a key step. J Org Chem. 2010 May 7;75 (9) :3105-8.|[3]Curir P, et al. 3-Hydroxyacetophenone in carnations is a phytoanticipin active against Fusarium oxysporum f. sp. dianthi. Phytochemistry, 1996, 41 (2) : 447-450.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference Standards
  • CAS Number:

    [121-71-1]