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4-(2,3-Dihydroxy-3-methylbutoxy)-7H-furo[3,2-g][1]benzopyran-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24724-52-5

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24724-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24724-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,2 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24724-52:
(7*2)+(6*4)+(5*7)+(4*2)+(3*4)+(2*5)+(1*2)=105
105 % 10 = 5
So 24724-52-5 is a valid CAS Registry Number.

24724-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

1.2 Other means of identification

Product number -
Other names oxypeucedacin

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:24724-52-5 SDS

24724-52-5Relevant academic research and scientific papers

Benzofuran and coumarin derivatives from the root of Angelica dahurica and their PPAR-γ ligand-binding activity

Matsuo, Yukiko,Yamaguchi, Emi,Hakamata, Ryo,Ootomo, Kanae,Takatori, Kazuhiro,Fukaya, Haruhiko,Mimaki, Yoshihiro

, (2020/02/26)

A phytochemical investigation of the root of Angelica dahurica led to the isolation of benzofuran and coumarin derivatives. This is the first report of the isolation and identification of three furanocoumarin sulfates from A. dahurica root. The structures of a total of twelve undescribed compounds were determined by extensive spectroscopic analysis, including 2D NMR data, hydrolysis, and solvolysis, followed by either physicochemical and spectroscopic data or X-ray crystallographic analysis. The isolated compounds were evaluated for their PPAR-γ ligand-binding activity, and six compounds showed significant PPAR-γ ligand-binding activity. In particular, the undescribed benzofuran derivative, 3-[6,7-furano-9-hydroxy-4-(2″,3″-dihydroxy-3″-methylbutyloxy)]-phenyl propionic acid, exhibited the most potent PPAR-γ ligand-binding activity and accumulated intracellular lipid in 3T3-L1 cells.

Design, synthesis and evaluation of furanocoumarin monomers as inhibitors of CYP3A4

Row,Brown,Stachulski,Lennard

, p. 1604 - 1610 (2008/02/03)

A number of furanocoumarins isolated from grapefruit juice have been found to inhibit CYP3A4 activity in vitro. In this study, we have designed and synthesised a range of analogues based on bergamottin to investigate the relationship between chemical stru

Nonvolatiles of commercial lime and grapefruit oils separated by high-speed countercurrent chromatography

Feger, Wolfgang,Brandauer, Herbert,Gabris, Paulina,Ziegler, Herta

, p. 2242 - 2252 (2007/10/03)

The nonvolatile fractions of cold-pressed peel oils of Key and Persian lime as well as grapefruit were separated by high-speed countercurrent chromatography (HS-CCC). In addition to the isolation of the main coumarins, psoralens and polymethoxyflavones, a

Coumarins from Ferulago capillaris and F. brachyloba

Jimenez, Benedicto,Grande, Maria Concepcion,Anaya, Josefa,Torres, Pascual,Grande, Manuel

, p. 1025 - 1031 (2007/10/03)

Four new coumarins, (+)-senecioylprangol, (-)-3'-senecioyloxymarmesin, (+)-3'-hydroxyprantschimgin and (+)-2''-senecioyloxymarmesin, besides 12 known coumarins have been isolated from two Ferulago species. Their structures have been established by spectroscopic methods and partial synthesis. New synthetic 3'-oxocoumarins are also described. There is a remarkable difference in the contents of the most abundant coumarins found in the roots of both species: osthol and aurapten are specific to F. capillaris and F. brachyloba, respectively. (C) 2000 Elsevier Science Ltd.

STEROIDS, CHROMONE AND COUMARINS FROM ANGELICA OFFICINALIS

Harkar, S.,Razdan, T. K.,Waight, E. S.

, p. 419 - 426 (2007/10/02)

From the ethyl acetate extract of the fresh roots of Angelica officinalis var. himaliaca, besides sitosterol, pregnenolone, peucenin-7-methyl ether, osthol and 18 furanocoumarins have been characterized by spectroscopic methods, including 13C NMR, and some chemical transformations. - Keywords: Angelica officinalis; Umbelliferae; root; pregnenolone; sitosterol; osthol; peucenin-7-methyl ether; furanocoumarins.

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