Crocatone

CAS# 19937-86-1

Crocatone

2D Structure

Catalog No. BCN3532----Order now to get a substantial discount!

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3D structure

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Crocatone

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Chemical Properties of Crocatone

Cas No. 19937-86-1 SDF Download SDF
PubChem ID 177099 Appearance Powder
Formula C11H12O4 M.Wt 208.2
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1-(7-methoxy-1,3-benzodioxol-5-yl)propan-1-one
SMILES CCC(=O)C1=CC2=C(C(=C1)OC)OCO2
Standard InChIKey VQZAATPWXSLYBI-UHFFFAOYSA-N
Standard InChI InChI=1S/C11H12O4/c1-3-8(12)7-4-9(13-2)11-10(5-7)14-6-15-11/h4-5H,3,6H2,1-2H3
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 Crocatone

The roots of Anthriscus sylvestris

Biological Activity of Crocatone

DescriptionCrocatone is a natural product from Anthriscus sylvestris.

Protocol of Crocatone

Structure Identification
Journal of the Pharmaceutical Society of Japan, 1978 , 98 :1486-1490.

Chemical Components of the Roots of Anthriscus sylvestris HOFFM. I. Structures of an Acyloxycarboxylic Acid and a New Phenylpropanoidester, Anthriscusin[Reference: WebLink]


METHODS AND RESULTS:
An acyloxycarboxylic acid (V), a new phenylpropanoid ester, anthriscusin (VI), and a phenylpropanoid ester (VII) were isolated from the roots of Anthriscus sylvestris HOFFM. (Umbelliferae), together with three kinds of known lignans, anthricin (I), isoanthricin (II) and 2-(3", 4", 5"-trimethoxybenzyl)-3-(3', 4'-methylenedioxybenzyl) butyrolactone (III), and a known phenylpropanoid, Crocatone (IV).
CONCLUSIONS:
The structures of V and VI were elucidated respectively as (Z)-2-angeloyloxymethyl-2-butenoic acid and O-[(Z)-2-angeloyloxymethyl-2-butenoyl]-3-methoxy-4,5-methylenedioxycinnamyl alcohol, and the structure of VII was presumed as 1-(3-methoxy-4,5-methylenedioxyphenyl)-2-angeloyloxypropan-1-one on the basis of its spectral data.

Crocatone Dilution Calculator

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Crocatone Molarity Calculator

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Preparing Stock Solutions of Crocatone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.8031 mL 24.0154 mL 48.0307 mL 96.0615 mL 120.0768 mL
5 mM 0.9606 mL 4.8031 mL 9.6061 mL 19.2123 mL 24.0154 mL
10 mM 0.4803 mL 2.4015 mL 4.8031 mL 9.6061 mL 12.0077 mL
50 mM 0.0961 mL 0.4803 mL 0.9606 mL 1.9212 mL 2.4015 mL
100 mM 0.048 mL 0.2402 mL 0.4803 mL 0.9606 mL 1.2008 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 Crocatone

[Chemical constituents from root of Angelica decursiva].[Pubmed:29139270]

Zhongguo Zhong Yao Za Zhi. 2017 Aug;42(15):2999-3003.

The compounds were isolated and purified by HP20 macroporous adsorption resin, ODS, silica gel, and Sephadex LH-20 column chromatography, as well as semi-preparative HPLC chromatography from the 80% ethanol extract of the root of Angelica decursiva, and their structures were identified based on their physiochemical properties and spectroscopic data. Twelve compounds were structures were identified as (9R,10R)-9-acetoxy-8,8-dimethyl-9,10-dihydro-2H,8H-benzo[1,2-b3,4-b']dipyran-2-on e-10-yl ester (1), bakuchicin (2), (3', S,4'S)-disenecioyloxy-3',4'-dihydroseselin (3), (3'R,4'R)-3'-angeloyloxy-4'-senecioyloxy-3',4'-dihydroseselincalipteryxin (4), (+)-8,9-dihydro-8-(2-hydroxypropan-2-yl)-2-oxo-2H-furo[2,3h]chromen-9-yl-3-methyl but-2-enoate (5), libanoridin (6), selinidin (7), suberosin (8), Crocatone (9), peujaponisinol B (10), peujaponisinol A (11), and ostenol (12), respectively. Compounds 1-5 were isolated from the plants of Angelica genus for the first time. Compounds 7-12 were isolated from A. decursiva for the first time.

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