3-(4-Hydroxyphenyl)-1-propanol

3-(4-Hydroxyphenyl)-1-propanol
Product Name 3-(4-Hydroxyphenyl)-1-propanol
CAS No.: 10210-17-0
Catalog No.: CFN99037
Molecular Formula: C9H12O2
Molecular Weight: 152.2 g/mol
Purity: >=98%
Type of Compound: Phenylpropanoids
Physical Desc.: Oil
Source: The fruits of Zanthoxylum cuspidatum
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
3-(4-Hydroxyphenyl)-1-propanol has a certain degree of regulation of plant growth and development.
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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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  • 3-(4-Hydroxyphenyl)-1-propanol

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    METHODS AND RESULTS:
    (-)-Monoterpenylmagnolol (3) was synthesized in eight steps from (+)-3,9-dibromocamphor (4) and the bis(methoxymethyl) ether (22) of 3-(4-Hydroxyphenyl)-1-propanol. Fragmentation of an endo-3-aryl-9-bromocamphor (27) provided the correct absolute stereochemistry. In this total synthesis, dissolving metal conditions were developed to reduce enol phosphate and isopropenyl functions without concomitant reduction of an attached phenol. Palladium(O)-catalyzed cross-coupling of an arylzinc chloride with 4-allyl-2-iodophenyl methoxymethyl ether (34) provided the desired tricyclic 1,2,3,5-tetrasubstituted biaryl 41 in fair yield without optimization and with little isomerization of the allyl group.
    CONCLUSIONS:
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