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1617-49-8

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1617-49-8 Usage

General Description

3,7,8-tri-O-methylellagic acid is a natural compound found in various plant sources, including berries, nuts, and fruits. It is a derivative of ellagic acid, a polyphenolic compound known for its antioxidant and anti-inflammatory properties. 3,7,8-tri-O-methylellagic acid has been studied for its potential health benefits, including its ability to inhibit the growth of cancer cells and reduce inflammation. It has also been investigated for its potential role in protecting against cardiovascular diseases and neurodegenerative disorders. Additionally, this compound has shown promising results in promoting skin health and protecting against UV-induced damage. Overall, 3,7,8-tri-O-methylellagic acid is a promising natural compound with potential therapeutic applications in various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1617-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1617-49:
(6*1)+(5*6)+(4*1)+(3*7)+(2*4)+(1*9)=78
78 % 10 = 8
So 1617-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H12O8/c1-21-9-5-7-11-10-6(16(19)25-15(11)13(9)23-3)4-8(18)12(22-2)14(10)24-17(7)20/h4-5,18H,1-3H3

1617-49-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ELLAGIC ACID, 3,3',4-TRI-O-METHYL

1.2 Other means of identification

Product number -
Other names 3,4,3'-tri-O-methylellagic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1617-49-8 SDS

1617-49-8Downstream Products

1617-49-8Relevant articles and documents

Tannins and related polyphenols of euphorbiaceous plants. XI. Three new hydrolyzable tannins and a polyphenol glucoside from Euphorbia humifusa

Yoshida,Amakura,Liu,Okuda

, p. 1803 - 1807 (1994)

Three new hydrolyzable tannins, euphormisins M1, M2 and M3, were isolated from Euphorbia humifusa Willd., and respectively characterized as 1,3,6-tri-O-galloyl-4-O-brevifolincarboxyl-β-D-glucose (19), an oxidative metabolite (23) of geraniin, and 1,3,6-tri-O-galloyl-α-D-glucose (18), by spectroscopic and chemical methods. A new ellagic acid glucoside (16) and fifteen known tannins, including geraniin (8) and four dimers [euphorbins A (13), B (14), excoecarianin (15) and eumaculin A (12)], were also isolated.

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Row,Rao

, p. 357 (1962)

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Ellagic acid glycosides with hepatoprotective activity from traditional Tibetan medicine Potentilla anserina

Morikawa, Toshio,Imura, Katsuya,Akagi, Yoshinori,Muraoka, Osamu,Ninomiya, Kiyofumi

, p. 317 - 325 (2017/10/17)

Two new gallic acid glycosides, potentillanosides G (1) and H (2), were newly isolated from the methanol extract of the tuberous roots of Potentilla anserina (Rosaceae), together with a known compound, ellagic acid 3-O-α-l-rhamnopyranoside (3). Their structures were elucidated on the basis of chemical and physicochemical evidence. Among the constituents, potentillanoside H (2, IC50?=?99.5?μM) was found to show hepatoprotective activity.

Total synthesis of 3,3′,4-tri-O-methylellagic acid from gallic acid

Alam, Ashraful,Tsuboi, Sadao

, p. 10454 - 10465 (2008/02/12)

Total synthesis of 3,3′,4-tri-O-methylellagic acid has been described from commercially available gallic acid. Construction of the crucial unsymmetric Ar-Ar bond has been carried out in various methods such as Heck coupling, Heck coupling followed by oxidation or anionic Fries rearrangement, Suzuki cross-coupling, etc., but all the attempts were unsuccessful. Then, finally it has been achieved by intramolecular Ullmann coupling reaction.

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