Amabiline

Amabiline
Product Name Amabiline
CAS No.: 17958-43-9
Catalog No.: CFN00236
Molecular Formula: C15H25NO4
Molecular Weight: 283.37 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Cynoglossum amabile
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.
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    CAS No: 17958-43-9
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    Org Lett. 2012 Apr 6;14(7):1869-71.
    Enantioselective total synthesis of (+)-amabiline.[Pubmed: 22432912 ]

    METHODS AND RESULTS:
    The first total synthesis of (+)-Amabiline, an unsaturated pyrrolizidine alkaloid from Cynoglossum amabile, is reported. This convergent, enantioselective synthesis proceeds in 15 steps (10-step longest linear sequence) in 6.2% overall yield and features novel methodology to construct the unsaturated pyrrolizidine or (-)-supinidine core.
    Org Lett. 2009 Jul 16;11(14):3160-2.
    A chemoenzymatic total synthesis of (+)-amabiline.[Pubmed: 19586069]

    METHODS AND RESULTS:
    The readily available and enzymatically derived cis-1,2-dihydrocatechol 3 has been converted, over 15 steps, into (+)-Amabiline, the non-natural enantiomeric form of a crinine-type alkaloid.
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