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1,4-Anthracenedione,5,10-dihydroxy-7-methoxy-2-methyl-

Base Information Edit
  • Chemical Name:1,4-Anthracenedione,5,10-dihydroxy-7-methoxy-2-methyl-
  • CAS No.:74815-58-0
  • Molecular Formula:C16H12 O5
  • Molecular Weight:284.268
  • Hs Code.:
  • Mol file:74815-58-0.mol
1,4-Anthracenedione,5,10-dihydroxy-7-methoxy-2-methyl-

Synonyms:Isoviocristin

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Chemical Property of 1,4-Anthracenedione,5,10-dihydroxy-7-methoxy-2-methyl- Edit
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Technology Process of 1,4-Anthracenedione,5,10-dihydroxy-7-methoxy-2-methyl-

There total 1 articles about 1,4-Anthracenedione,5,10-dihydroxy-7-methoxy-2-methyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; In dimethyl sulfoxide; for 0.0333333h;
DOI:10.1002/jlac.198219821210
upstream raw materials:

physcion-9-anthrone

Refernces Edit

Metabolic products of microorganisms. 214. Viocristin, isoviocristin, and hydroxyviocristin. Structure and synthesis of naturally occurring 1,4-anthraquinones

10.1002/jlac.198219821210

The research focuses on the metabolic products of the fungus Aspergillus cristatus, specifically the identification and synthesis of naturally occurring 1,4-anthraquinones, including Viocristin (19a), Isoviocristin (18a), and Hydroxyviocristin (13). These compounds are unique as they belong to the 1,4-anthraquinone series, which had not been previously found in nature. The study involved the isolation of these pigments from the mycelium of A. cristatus and detailed their chemical structures through various spectroscopic methods, such as mass spectrometry, 'H-NMR, and IR spectroscopy. The researchers also synthesized these compounds and several model compounds to confirm their structures and to explore their biological activities. Key chemicals involved in the research include Acetanhydride, Methyliodide, Sodium hydroxide, and Dimethyl sulfoxide, which were used in various reactions to synthesize and modify the anthraquinones. The research also utilized solvents like Chloroform, Methanol, and Ethyl acetate for dissolving and crystallizing the compounds. The study provides insights into the biosynthetic pathways of these compounds and their potential applications, particularly in the context of their antimicrobial properties demonstrated in the plate diffusion test.

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