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52591-10-3

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52591-10-3 Usage

Preparation

Preparation by reaction of p-hydroxybenzonitrile with phloroglucinol, (15%) (Hoesch reaction).

Check Digit Verification of cas no

The CAS Registry Mumber 52591-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,9 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52591-10:
(7*5)+(6*2)+(5*5)+(4*9)+(3*1)+(2*1)+(1*0)=113
113 % 10 = 3
So 52591-10-3 is a valid CAS Registry Number.

52591-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Hydroxyphenyl)(2,4,6-trihydroxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names Methanone, (4-hydroxyphenyl)(2,4,6-trihydroxyphenyl)-

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:52591-10-3 SDS

52591-10-3Relevant articles and documents

Laxative effect of agarwood leaves and its mechanism

Hara, Hideaki,Ise, Yasuaki,Morimoto, Nobutaka,Shimazawa, Masamitsu,Ichihashi, Koji,Ohyama, Masayoshi,Iinuma, Munekazu

, p. 335 - 345 (2008)

We investigated the laxative activity of an extract of agarwood leaves from Aquilaria sinensis. The laxative activity was measured in mice by counting the stool frequency and stool weight, and the drugs were orally administered. An acetone extract of agar

Bio-assay guided isolation and identification of α-glucosidase inhibitors from the leaves of Aquilaria sinensis

Feng, Jie,Yang, Xiu-Wei,Wang, Ru-Feng

experimental part, p. 242 - 247 (2011/10/12)

Eight α-glucosidase inhibitors including four new compounds were isolated from the 70% aqueous ethanolic extract of leaves of Aquilaria sinensis (Lour.) Gilg by activity-directed fractionation and purification processes. The ethanolic extract was first separated into petroleum ether, ethyl acetate, n-butanol and water soluble fractions and screened for inhibitory activity against α-glucosidase. Further activity-directed investigation lead to the isolation of four new compounds with moderate inhibitory activity, viz, aquilarisinin (1), aquilarisin (2), hypolaetin 5-O-β-d-glucuronopyranoside (3) and aquilarixanthone (4) from the n-butanol fraction, and four known compounds showing potent activity including mangiferin (5), iriflophenone 2-O-α-l-rhamnopyranoside (6), iriflophenone 3-C-β-d-glucoside (7) and iriflophenone 3,5-C-β-d-diglucopyranoside (8) from the most potent ethyl acetate fraction. The structures of these compounds were determined by extensive spectroscopic analyses, including IR, UV, ESIMS, HRESIMS, 1D and 2D NMR.

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