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23513-13-5

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23513-13-5 Usage

General Description

(E)-1-(4-hydroxy-3-methoxyphenyl)dec-4-en-3-one is a chemical compound with a long and complex name. It is an unsaturated ketone that contains a hydroxy group and a methoxy group, as well as a phenyl ring. (E)-1-(4-hydroxy-3-methoxyphenyl)dec-4-en-3-one is commonly found in various plants and natural products, and it possesses antioxidant and anti-inflammatory properties. It has been studied for its potential therapeutic effects in various diseases and conditions, and it is also used in the production of flavors, fragrances, and pharmaceuticals. Overall, (E)-1-(4-hydroxy-3-methoxyphenyl)dec-4-en-3-one is a versatile and important chemical compound with various potential applications in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 23513-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,1 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23513-13:
(7*2)+(6*3)+(5*5)+(4*1)+(3*3)+(2*1)+(1*3)=75
75 % 10 = 5
So 23513-13-5 is a valid CAS Registry Number.

23513-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6)-shogaol

1.2 Other means of identification

Product number -
Other names (E)-1-(4'-hydroxy-3'-methoxyphenyl)-4-decen-3-one

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:23513-13-5 SDS

23513-13-5Relevant articles and documents

First enantioselective synthesis of gingesulfonic acids and unequivocal determination of their absolute stereochemistry

Adamo, Mauro F. A.,Bencivenni, Grazia,Gillick-Healy, Malachi W.,Kelly, Brian G.,Moccia, Maria,Ravelli, Andrea

supporting information, p. 1091 - 1094 (2020/02/22)

Herein we report the first organocatalysed enantioselective synthesis of gingesulfonic acids and shogasulfonic acids via a mild and convenient aminothiourea-catalysed conjugate addition of bisulfite to the olefin moiety of α,β-unsaturated carbonyls - a technology previously reported by us. A series of optically active naturally occurring sulfonic acids are prepared in their natural and unnatural configurations, and their absolute configurations are unequivocally confirmed by single crystal X-ray diffractometry.

Influence of side chain structure changes on antioxidant potency of the [6]-gingerol related compounds

Lu, Dong-Liang,Li, Xiu-Zhuang,Dai, Fang,Kang, Yan-Fei,Li, Yan,Ma, Meng-Meng,Ren, Xiao-Rong,Du, Gao-Wei,Jin, Xiao-Ling,Zhou, Bo

, p. 191 - 197 (2014/06/24)

[6]-Gingerol and [6]-shogaol are the major pungent components in ginger with a variety of biological activities including antioxidant activity. To explore their structure determinants for antioxidant activity, we synthesized eight compounds differentiated by their side chains which are characteristic of the C1-C2 double bond, the C4-C5 double bond or the 5-OH, and the six- or twelve-carbon unbranched alkyl chain. Our results show that their antioxidant activity depends significantly on the side chain structure, the reaction mediums and substrates. Noticeably, existence of the 5-OH decreases their formal hydrogen-transfer and electron-donating abilities, but increases their DNA damage- and lipid peroxidation-protecting abilities. Additionally, despite significantly reducing their DNA strand breakage-inhibiting activity, extension of the chain length from six to twelve carbons enhances their anti-haemolysis activity.

Protection-, salt-, and metal-free syntheses of [n]-shogaols by use of dimethylammonium dimethyl carbamate (DIMCARB) without protecting groups

Mase, Nobuyuki,Kitagawa, Norihiko,Takabe, Kunihiko

experimental part, p. 93 - 96 (2010/07/16)

Shogaols, the pungent principle of ginger, exhibit interesting bioactivities. Practical preparation of shogaols is highly desired. Here we report the protection/deprotection-, salt-, and metalfree synthesis of shogaol in three steps by use of dimethylammonium dimethyl carbamate (DIMCARB), in which DIMCARB smoothly promoted Mannich-type condensation of the ketone donor with the aldehyde acceptor through the iminium cation intermediate. Georg Thieme Verlag Stuttgart.

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