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Androsin is a complex chemical compound that serves as an insect antifeedant, naturally occurring in the roots of the plant Adenostyles alliariae, which belongs to the Asteraceae family and is predominantly found in Europe. This organic compound is an active constituent of androsin sesquiterpene lactone, which possesses toxic properties and a unique trait of deterring insects, making it a potent biocontrol agent. The framework of androsin consists of sesquiterpene lactone, a compound with known pharmacological properties.

531-28-2

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531-28-2 Usage

Uses

Used in Agricultural Industry:
Androsin is used as a biocontrol agent for enhancing the plant's resistance against herbivores. Its notable insect deterrent activity creates an invincible protective barrier, reducing the need for chemical pesticides and promoting sustainable agriculture.
Used in Pharmaceutical Industry:
Androsin is used as a potential pharmaceutical candidate due to its toxic properties and pharmacological activities. The sesquiterpene lactone framework of androsin offers opportunities for the development of new drugs, particularly in the area of pest control and insect repellents.
Used in Insect Repellent Products:
Androsin is used as an active ingredient in insect repellent products, providing a natural and effective solution to deter insects and protect against insect-borne diseases. Its unique insect deterrent activity makes it a valuable component in the formulation of eco-friendly insect repellents.

Check Digit Verification of cas no

The CAS Registry Mumber 531-28-2 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, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 531-28:
(5*5)+(4*3)+(3*1)+(2*2)+(1*8)=52
52 % 10 = 2
So 531-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O8/c1-7(17)8-3-4-9(10(5-8)21-2)22-15-14(20)13(19)12(18)11(6-16)23-15/h3-5,11-16,18-20H,6H2,1-2H3/t11-,12-,13+,14-,15-/m1/s1

531-28-2SDS

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 1-[3-methoxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethy l)tetrahydropyran-2-yl]oxy-phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 1-(4-trifluoromethyl-pyrimidin-2-yl)-piperidine-4-carbonyl chloride

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:531-28-2 SDS

531-28-2Relevant academic research and scientific papers

NEW SYNTHESES OF PLANT ARYL GLYCOSIDES AS POTENTIAL GENE INDUCERS

Delay, Didier,Delmotte, Francis

, p. 223 - 234 (2007/10/02)

Aryl β-D-glycopyranosides have been synthesized by coupling acetovanillone (4-hydroxy-3-methoxyacetophenone) with D-glucose, D-galactose, and maltose; acetosyringone (4-hydroxy-3,5-dimethoxyacetophenone) with D-glucose and D-galactose; syringaldehyde (3-methoxyvanillin) with D-glucose; and syringic acid (4-hydroxy-3,5-dimethoxybenzoic acid) with D-glucose.The Mauthner's procedure using peracetylated glycosyl bromides and phenolates in aqueous acetone afforded the acetylated β-D-glycosides, which were deacetylated.

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