Physoperuvine

Physoperuvine
Product Name Physoperuvine
CAS No.: 60723-27-5
Catalog No.: CFN00221
Molecular Formula: C8H15NO
Molecular Weight: 141.21 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Oil
Source: The herbs of Physalis peruviana Linne
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Reference standards.
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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.
  • Nutrients.2019, 12(1)
  • Phytochemistry Letters2015, 243-247
  • J Agric Food Chem.2021, 69(11):3496-3510.
  • Food Chem.2024, 452:139555.
  • Molecules.2023, 28(8):3503.
  • PLoS One.2022, 17(4):e0267007.
  • Molecules.2023, 28(18):6734.
  • Indian J Pharm Sci.2022, 84(4): 874-882.
  • J Sci Food Agric.2024, 104(7):4425-4437.
  • Nutrients.2021, 13(8):2901.
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    A stereoselective synthesis of (+)-physoperuvine using a tandem aza-Claisen rearrangement and ring closing metathesis reaction.[Pubmed: 19532981]

    METHODS AND RESULTS:
    A stereoselective synthesis of (+)-Physoperuvine, a tropane alkaloid from Physalis peruviana Linne has been developed using a one-pot tandem aza-Claisen rearrangement and ring closing metathesis reaction to form the key amino-substituted cycloheptene ring.
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