2-Methoxyphenalen-1-one

2-Methoxyphenalen-1-one
Product Name 2-Methoxyphenalen-1-one
CAS No.: 51652-39-2
Catalog No.: CFN96874
Molecular Formula: C14H10O2
Molecular Weight: 210.23 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Oil
Targets: Antifection
Source: The rhizomes of Musa acuminata var.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
2-Methoxy-1H-phenalen-1-one (2-Methoxyphenalen-1-one) displays significantly enhanced activity against Mycosphaerella fijiensis in comparison with other phenylphenalenones.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    J Nat Prod. 2007 May;70(5):887-90.
    Phenalenone-type compounds from Musa acuminata var. [Pubmed: 17428093 ]

    METHODS AND RESULTS:
    Two perinaphthenone-type compounds (1 and 2) were isolated together with four known phenylphenalenones (3-6) from the rhizomes of Musa acuminata var. "Yangambi km 5". The structures of the new phenalenones were assigned as 2-hydroxy-1H-phenalen-1-one (1) and 2-methoxy-1H-phenalen-1-one (2-Methoxyphenalen-1-one ,2) on the basis of their spectroscopic data and were confirmed by synthesis.
    CONCLUSIONS:
    Compounds 1 and 2 displayed significantly enhanced activity against Mycosphaerella fijiensis in comparison with other phenylphenalenones.
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