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
531-28-2Relevant 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.