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531-44-2

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531-44-2 Usage

Uses

Scopoletin 7-O-glucoside is a derivative of Scopoletin (S200500), a common constituent found in a variety of plants that has potential to regulate hyperthyroidism in rats. Scopoletin 7-O-glucoside is a compound that is obtained from the methanolic extract of the fresh underground parts of the flower Scopolia japonica.

Definition

ChEBI: A member of the class of coumarins that is scopoletin attached to a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage.

Check Digit Verification of cas no

The CAS Registry Mumber 531-44-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 531-44:
(5*5)+(4*3)+(3*1)+(2*4)+(1*4)=52
52 % 10 = 2
So 531-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H18O9/c1-22-9-4-7-2-3-12(18)23-8(7)5-10(9)24-16-15(21)14(20)13(19)11(6-17)25-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13-,14+,15-,16?/m1/s1

531-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name scopolin

1.2 Other means of identification

Product number -
Other names Murrayin

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:531-44-2 SDS

531-44-2Relevant articles and documents

COUMARINS OF Haplophyllum obtusifolium. STRUCTURES OF TWO NEW COUMARIN GLYCOSIDES

Batirov, E. Kh.,Matkarimov, A. D.,Malikov, V. M.,Seitmuratov, E.

, p. 654 - 657 (2007/10/02)

Two coumarin glycosides have been isolated from an aqueous ethanolic extract of the epigeal part of Haplophyllum obtusifolium: (I) - C16H16O10, mp 164-166 deg C, D -52.4 deg (dimethylformamide); and (II) - C26H26O12, mp 206-208 deg C, D -110.5 deg (pyridine).It has been established on the basis of chemical transformations and spectral characteristics that (I) has the structure of fraxetin 7-O-β-D-glucopyranoside and (II) that of scopoletin 7-O-(6'-O-feruloyl-β-D-glucopyranoside).

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