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Catalog Number:
24118
CAS Number:
20007-72-1
(±)-8a-méthyl-3,4,8,8a-tétrahydro-1,6(2 H ,7 H )-naphtalènedione
Purity:
≥ 99 % (HPLC)
Synonym(s):
(+/-)-9-méthyl-5(10)-octaline-1,6-dione, Cétone de Wieland-Miescher
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Product Information

L'énolate formé avec le LDA subit une double réaction de Michael avec l'acrylate de méthyle pour donner un produit tricyclique. Tetrahedron, 51, 9891 (1995)

Synonyms
(+/-)-9-méthyl-5(10)-octaline-1,6-dione, Cétone de Wieland-Miescher
CAS Number
20007-72-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C11H14O2
Molecular Weight
178.23
MDL Number
MFCD00001687
PubChem ID
89262
Melting Point
48 - 50 ?C
Appearance
Solide jaune pâle
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
(+/-)-9-méthyl-5(10)-octaline-1,6-dione, Cétone de Wieland-Miescher
CAS Number
20007-72-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C11H14O2
Molecular Weight
178.23
MDL Number
MFCD00001687
PubChem ID
89262
Melting Point
48 - 50 ?C
Appearance
Solide jaune pâle
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Wieland-Miescher ketone is widely utilized in research focused on:

  • Synthesis of Natural Products: This compound serves as a key intermediate in the synthesis of various natural products, enabling researchers to create complex molecules with potential therapeutic properties.
  • Pharmaceutical Development: Its unique structure allows for the development of new pharmaceuticals, particularly in the fields of oncology and infectious diseases, where innovative compounds are crucial.
  • Organic Chemistry Research: It is often used in organic synthesis as a building block, facilitating the creation of diverse chemical libraries for drug discovery.
  • Material Science: Wieland-Miescher ketone can be employed in the development of novel materials, including polymers and coatings, which benefit from its chemical properties.
  • Biochemical Studies: Researchers utilize this compound to study enzyme interactions and metabolic pathways, providing insights into biological processes and potential drug targets.

Citations