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p-Hydroxyphenethyl anisate

CAS# 87932-34-1

p-Hydroxyphenethyl anisate

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p-Hydroxyphenethyl anisate: 5mg $213 In Stock
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Quality Control of p-Hydroxyphenethyl anisate

Number of papers citing our products

Chemical structure

p-Hydroxyphenethyl anisate

3D structure

Chemical Properties of p-Hydroxyphenethyl anisate

Cas No. 87932-34-1 SDF Download SDF
PubChem ID 14704104 Appearance Powder
Formula C16H16O4 M.Wt 272.30
Type of Compound Phenols Storage Desiccate at -20°C
Synonyms 4-Hydroxyphenethylanisate
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-(4-hydroxyphenyl)ethyl 4-methoxybenzoate
SMILES COC1=CC=C(C=C1)C(=O)OCCC2=CC=C(C=C2)O
Standard InChIKey DSMAYKYXHOGICG-UHFFFAOYSA-N
Standard InChI InChI=1S/C16H16O4/c1-19-15-8-4-13(5-9-15)16(18)20-11-10-12-2-6-14(17)7-3-12/h2-9,17H,10-11H2,1H3
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of p-Hydroxyphenethyl anisate

The roots and rhizomes of Notopterygium incisum.

Biological Activity of p-Hydroxyphenethyl anisate

Descriptionp-Hydroxyphenethyl anisate is a natural product from Notopterygium incisum.

Protocol of p-Hydroxyphenethyl anisate

Structure Identification
Zhongguo Zhong Yao Za Zhi. 2008 Dec;33(24):2918-21.

Studies on chemical constituents in roots and rhizomes of Notopterygium incisum.[Pubmed: 19294850]

To study the chemical constituents in the roots and rhizomes of Notopterygium incisum.
METHODS AND RESULTS:
The chemical constituents were isolated by various column chromatographic methods and structurally elucidated by NMR and MS evidences. Twenty-four compounds were obtained and identified as isocalamenediol (1), pregnenolone (2), beta-sitosterol (3), bergapten (4), bergaptol (5), cnidilin (6), isoimperatorin (7), bergamottin (8), demethylfuropinnarin (9), nodakenetin (10), 7'-O-methylnotoptol (11), notopterol (12), notoptol (13), pabulenol (14), phenethylferulate (15), p-Hydroxyphenethyl anisate (16), trans-ferulic acid (17), nodakenin (18), sucrose (19), 2-methoxy-4-(3-methoxy-1-propenyl)-phenol (20), 3, 4, 5 trimethoxy-trans-cinnamic acid (21), p-methoxycinnamic acid (22), 4-acetoxy-3-methoxy-trans-cinnamic acid (23), and p-hydroxy-trans-cinnamic acid (24).

p-Hydroxyphenethyl anisate Dilution Calculator

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p-Hydroxyphenethyl anisate Molarity Calculator

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Preparing Stock Solutions of p-Hydroxyphenethyl anisate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.6724 mL 18.3621 mL 36.7242 mL 73.4484 mL 91.8105 mL
5 mM 0.7345 mL 3.6724 mL 7.3448 mL 14.6897 mL 18.3621 mL
10 mM 0.3672 mL 1.8362 mL 3.6724 mL 7.3448 mL 9.1811 mL
50 mM 0.0734 mL 0.3672 mL 0.7345 mL 1.469 mL 1.8362 mL
100 mM 0.0367 mL 0.1836 mL 0.3672 mL 0.7345 mL 0.9181 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on p-Hydroxyphenethyl anisate

[Studies on chemical constituents in roots and rhizomes of Notopterygium incisum].[Pubmed:19294850]

Zhongguo Zhong Yao Za Zhi. 2008 Dec;33(24):2918-21.

OBJECTIVE: To study the chemical constituents in the roots and rhizomes of Notopterygium incisum. METHOD: The chemical constituents were isolated by various column chromatographic methods and structurally elucidated by NMR and MS evidences. RESULT: Twenty-four compounds were obtained and identified as isocalamenediol (1), pregnenolone (2), beta-sitosterol (3), bergapten (4), bergaptol (5), cnidilin (6), isoimperatorin (7), bergamottin (8), demethylfuropinnarin (9), nodakenetin (10), 7'-O-methylnotoptol (11), notopterol (12), notoptol (13), pabulenol (14), phenethylferulate (15), p-Hydroxyphenethyl anisate (16), trans-ferulic acid (17), nodakenin (18), sucrose (19), 2-methoxy-4-(3-methoxy-1-propenyl)-phenol (20), 3, 4, 5 trimethoxy-trans-cinnamic acid (21), p-methoxycinnamic acid (22), 4-acetoxy-3-methoxy-trans-cinnamic acid (23), and p-hydroxy-trans-cinnamic acid (24). CONCLUSION: Compounds 1, 14, 20-24 were isolated from the roots and rhizomes of N. incisum for the first time. Compounds 1 and 14 are sesquiterpenoid and coumarin, respectively, and 20-24 were phenylpropanoid compounds.

Description

p-Hydroxyphenethyl anisate is a main constituent of Notopterygium Radix.

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