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112448-39-2

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  • ≥98% high purity high quality custom manufacturing natural extract 3'-Demethylnobiletin; 3'-Hydroxy-5,6,7,8,4'-pentamethoxyflavone 112448-39-2

    Cas No: 112448-39-2

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112448-39-2 Usage

General Description

3'-Demethylnobiletin is a chemical compound that belongs to the flavonoid class of phytonutrients. It is a natural derivative of nobiletin, commonly found in citrus fruits and their extracts. 3'-Demethylnobiletin has been studied for its potential health benefits, including anti-inflammatory, anti-cancer, and neuroprotective properties. It is known for its ability to modulate various signaling pathways involved in cellular function and has shown promise in reducing oxidative stress and promoting overall wellness. Additionally, 3'-Demethylnobiletin has been investigated for its potential role in improving metabolic health and reducing the risk of chronic diseases such as diabetes and cardiovascular conditions. Overall, this chemical compound shows great potential for promoting health and wellbeing, making it an area of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 112448-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112448-39:
(8*1)+(7*1)+(6*2)+(5*4)+(4*4)+(3*8)+(2*3)+(1*9)=102
102 % 10 = 2
So 112448-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H20O8/c1-23-13-7-6-10(8-11(13)21)14-9-12(22)15-16(24-2)18(25-3)20(27-5)19(26-4)17(15)28-14/h6-9,21H,1-5H3

112448-39-2SDS

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 2-(3-hydroxy-4-methoxyphenyl)-5,6,7,8-tetramethoxychromen-4-one

1.2 Other means of identification

Product number -
Other names 4H-1-Benzopyran-4-one,2-(3-hydroxy-4-methoxyphenyl)-5,6,7,8-tetramethoxy

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:112448-39-2 SDS

112448-39-2Relevant articles and documents

Synthetic studies of fisetin, myricetin and nobiletin analogs and related probe molecules

Hiza, Aiki,Tsukaguchi, Yuta,Ogawa, Takahiro,Inai, Makoto,Asakawa, Tomohiro,Hamashima, Yoshitaka,Kan, Toshiyuki

, p. 1371 - 1396 (2016/10/12)

We synthesized a series of analogs of fisetin, myricetin and nobiletin, as well as related fluorescein- and biotin-based flavone-probe molecules, on a suitable scale for biological and structure-activity relationship studies.

Semisynthesis and antiproliferative evaluation of a series of 3′-aminoflavones

Quintin, Jerome,Buisson, Didier,Thoret, Sylviane,Cresteil, Thierry,Lewin, Guy

scheme or table, p. 3502 - 3506 (2010/04/26)

A series of 3′-aminoflavones 5,6,7,8-tetra- or 5,7-dioxygenated on the A-ring was synthesized from tangeretin or naringin, two natural Citrus flavonoids. These flavones were evaluated for antiproliferative activity, activation of apoptosis, and inhibition

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