3-(4-Hydroxyphenyl)-1-propanol | CAS:10210-17-0

3-(4-Hydroxyphenyl)-1-propanol

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Product Name	3-(4-Hydroxyphenyl)-1-propanol
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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.
Download:	COA MSDS SDF Manual
Similar structural:	Comparison (Web) (SDF)
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Size /Price /Stock	10 mM * 1 mL in DMSO / Inquiry
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3-(4-Hydroxyphenyl)-1-propanol Description

Source:	The fruits of Zanthoxylum cuspidatum
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	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
After receiving:	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.

Structure Identification:

Journal of Organic Chemistry, 1995, 60(6).

Synthesis of (-)-Monoterpenylmagnolol (XI) and Magnolol (XII).[Reference: WebLink]

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:
Magnolol (1) was also synthesized by aryl coupling of 34 and the methoxymethyl ether of 4-allyl-2-lithiophenol via the zinc chloride method as above, as well as from 5,5'-dibromo-2,2'-dimethoxybiphenyl (37) by allylation with allyltributylstannane followed by ether cleavage.

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Growth-promoting effects Compound Library Phenylpropanoids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	6.5703 mL	32.8515 mL	65.703 mL	131.406 mL	164.2576 mL
5 mM	1.3141 mL	6.5703 mL	13.1406 mL	26.2812 mL	32.8515 mL
10 mM	0.657 mL	3.2852 mL	6.5703 mL	13.1406 mL	16.4258 mL
50 mM	0.1314 mL	0.657 mL	1.3141 mL	2.6281 mL	3.2852 mL
100 mM	0.0657 mL	0.3285 mL	0.657 mL	1.3141 mL	1.6426 mL

CFN89230	4-Methoxycinnamyl alcohol	53484-50-7	164.20	C₁₀H₁₂O₂
CFN92410	trans-3,4-Methylenedioxycinnamyl alcohol	58095-76-4	178.2	C₁₀H₁₀O₃
CFN97760	Coniferyl alcohol	32811-40-8	180.20	C₁₀H₁₂O₃
CFN96742	Dihydroconiferyl alcohol	2305-13-7	182.21	C₁₀H₁₄O₃
CFN96094	Gamma-Methoxyisoeugenol	63644-71-3	194.2	C₁₁H₁₄O₃
CFN96771	Acetylisoeugenol	93-29-8	206.24	C₁₂H₁₄O₃
CFN98088	beta-Hydroxypropiovanillone	2196-18-1	196.2	C₁₀H₁₂O₄
CFN94482	Dihydrosinapylalcohol	20736-25-8	212.24	C₁₁H₁₆O₄
CFN97826	3,4'-Dihydroxy-3',5'-dimethoxypropiophenone	136196-47-9	226.23	C₁₁H₁₄O₅
CFN98379	3,4,5-Trimethoxycinnamyl alcohol	30273-62-2	224.3	C₁₂H₁₆O₄