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5-Acetyl-2-(1-hydroxy-1-methylethyl)benzofuran
5-Acetyl-2-(1-hydroxy-1-methylethyl)benzofuran
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 5-Acetyl-2-(1-hydroxy-1-methylethyl)benzofuran
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CAS No.: 64165-99-7
Catalog No.: CFN89200
Molecular Formula: C13H14O3
Molecular Weight: 218.25 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Source: The cultures of the inoculation of sliced yacon tubers with Pseudomonas cichorii.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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Product Use Citation
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: 5-Acetyl-2-(1-hydroxy-1-methylethyl)benzofuran is a phytoalexin.
5-Acetyl-2-(1-hydroxy-1-methylethyl)benzofuran Description
Source: The cultures of the inoculation of sliced yacon tubers with Pseudomonas cichorii.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: 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.

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After receiving: 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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Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.5819 mL 22.9095 mL 45.819 mL 91.638 mL 114.5475 mL
5 mM 0.9164 mL 4.5819 mL 9.1638 mL 18.3276 mL 22.9095 mL
10 mM 0.4582 mL 2.291 mL 4.5819 mL 9.1638 mL 11.4548 mL
50 mM 0.0916 mL 0.4582 mL 0.9164 mL 1.8328 mL 2.291 mL
100 mM 0.0458 mL 0.2291 mL 0.4582 mL 0.9164 mL 1.1455 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Phytochemistry, 1996, 43(5):1019-1021.
Three 4′-hydroxyacetophenone-related phytoalexins from Polymnia sonchifolia.[Reference: WebLink]
Inoculation of sliced yacon tubers with Pseudomonas cichorii resulted in the formation of antifungal compounds. Three major phytoalexins were isolated and identified by spectroscopic methods as 4′-hydroxy-3′-(3-methylbutanoyl)acetophenone, 4′-hydroxy-3′-(3-methyl-2-butenyl)acetophenone and 5-Acetyl-2-(1-hydroxy-1-methylethyl)benzofuran.
CFN983583,7,16-Trihydroxystigmast-5-ene289056-24-2446.7 C29H50O3
CFN95077Parvisoflavanone49776-79-6332.3C17H16O7
CFN90468Syringetin-3-O-glucoside40039-49-4508.43C23H24O13
CFN9935512-Ursene-3,16,22-triol1242085-06-8458.7 C30H50O3
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