1,7-Bis(4-hydroxyphenyl)hept-6-en-3-ol
1,7-Bis(4-hydroxyphenyl)hept-6-en-3-ol is a natural product from Alpinia galanga.
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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.
Environ Toxicol.2021, doi: 10.1002
Food Chem.2020, 332:127412
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Natural Product Sciences2024, 30(1):8-13.
Bioorg Med Chem.2020, 28(12):115553.
FUTURE VIROLOGYVOL.2023, 18(5).
Chinese Medicine2019, 14(1)
Separations2023, 10(2), 131.
J Agric Food Chem.2024, 72(40):22237-22249.
Nat Commun.2025, 16(1):4121.
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Helvetica Chimica Acta, 2012 , 95 (9) :1666-1671.
The First Stereoselective Total Synthesis of a Naturally Occurring BioactiveDiarylheptanoid, (3R,6E)-1,7-Bis(4-hydroxyphenyl)hept-6-en-3-ol, throughTwo Different Approaches1)[Reference:
WebLink]
The stereoselective total synthesis of a naturally occurring bioactive diarylheptanoid, (3R,6E)-1,7-Bis(4-hydroxyphenyl)hept-6-en-3-ol, has been accomplished starting from 4-hydroxybenzaldehydethrough two different approaches involving Wittig olefination, hydrolytic kinetic resolution of a racemicepoxide, and olefin cross-metathesis reaction as the key steps.
