1,3,3-Trimethyl-2-norbornanone

1,3,3-Trimethyl-2-norbornanone
Product Name 1,3,3-Trimethyl-2-norbornanone
CAS No.: 4695-62-9
Catalog No.: CFN70114
Molecular Formula: C10H16O
Molecular Weight: 152.2 g/mol
Purity: >=98%
Type of Compound: Monoterpenoids
Physical Desc.: Oil
Source:
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $30/20mg
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.

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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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    Journal of the Chemical Society, Perkin Transactions 1, 1976.
    Olefin synthesis by two-fold extrusion processes. Part 3. Synthesis and properties of hindered selenoketones (selones).[Reference: WebLink]

    METHODS AND RESULTS:
    Monomeric selenoketones (selones) have been prepared from di-t-butyl ketone and (–)-1,3,3-trimethylnorbornan-2-one( (–)-1,3,3-Trimethyl-2-norbornanone) through heating their triphenylphosphoranylidenehydrazones with selenium. Although selones show greater reactivity towards diazo-compounds than thiones it was still not possible to prepare the elusive tetra-t-butylethylene. However, (–)-1,1′,3,3,3′,3′-hexamethyl-2,2′-binorbornylidene, which is a 'tied back' tetra-t-butylethylene, was obtained without difficulty and is stable to oxygen.
    CONCLUSIONS:
    The chemistry of selones has been briefly explored and compared with that of thiones. An improved preparation of di-t-butylketen is reported.
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