546-09-8 Usage
Description
2β,7-Dihydroxy-1-methyl-8-methylenegibba-3,4a-diene-1α,10β-dicarboxylic acid is a complex organic compound characterized by its unique molecular structure, featuring a dicarboxylic acid backbone with multiple hydroxy and methyl groups. It belongs to the class of gibbane diterpenoids, which are known for their diverse biological activities and potential applications in various fields.
Used in Plant Growth Regulation:
2β,7-Dihydroxy-1-methyl-8-methylenegibba-3,4a-diene-1α,10β-dicarboxylic acid is used as a plant growth regulator for promoting growth and development in various plant species. It functions by mimicking the action of gibberellins, a group of plant hormones that stimulate cell elongation and division, leading to increased plant size and improved crop yields.
Used in Pharmaceutical Industry:
2β,7-Dihydroxy-1-methyl-8-methylenegibba-3,4a-diene-1α,10β-dicarboxylic acid is used as a pharmaceutical agent for its potential therapeutic effects. Its unique chemical structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs to treat a range of diseases.
Used in Cosmetics Industry:
2β,7-Dihydroxy-1-methyl-8-methylenegibba-3,4a-diene-1α,10β-dicarboxylic acid is used as an active ingredient in cosmetic products for its potential skin care benefits. Its ability to modulate cellular processes and interact with biological targets may contribute to improved skin health, appearance, and overall well-being.
Used in Agrochemical Industry:
2β,7-Dihydroxy-1-methyl-8-methylenegibba-3,4a-diene-1α,10β-dicarboxylic acid is used as an agrochemical for enhancing crop productivity and improving resistance to various environmental stresses. Its plant growth-regulating properties can be harnessed to develop novel agrochemical products that promote sustainable agriculture and food security.
Check Digit Verification of cas no
The CAS Registry Mumber 546-09-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 546-09:
(5*5)+(4*4)+(3*6)+(2*0)+(1*9)=68
68 % 10 = 8
So 546-09-8 is a valid CAS Registry Number.
546-09-8Relevant articles and documents
Selective deoxygenation of gibberellic acid with fluoroarylborane catalysts
Seo, Youngran,Gudz, Anton,Lowe, Jared M.,Gagné, Michel R.
, (2019)
Reductive late-stage functionalization of gibberellic acid is reported using three fluoroarylborane Lewis acids; (B(C6F5)3, B(3,5-C6H3(CF3)2), and B(2,4,6-C6H2F3)3) in combination with a tertiary silane and a borane (HBCat) reductant. In each case, C–O bond activation occurs, and different products are obtained depending on the reductant and catalyst employed.
PROOF OF FORMATION OF AN UNSTABLE CONJUGATED TRIENE ON DECOMPOSITION OF GIBBERELLIN A3 IN WATER
Pankrushina, N. A.,Tkachev, A. V.,Druganov, A. G.
, p. 630 - 634 (2007/10/02)
It has been shown by the methods of 1H NMR and high-performance liquid chromatography with recording of UV spectra that in aqueous solutions of gibberellin A3, via gibberellenic acid, an unstable conjugated triene having λmax 326 nm is formed which is readily converted into allogibberic acid and is isolated as a mixture (1:2) with this acid.In the 1H NMR spectrum of the triene, confirming its structure, spin-spin coupling both of the H-5 proton and of the protons of the methyl group with all the H-1, H-2, and the H-3 protons is observed.The precursor of allogibberic acid has been ascribed the structure of (-)-13-hydroxy-19,20-dinorgibberella-1,3,9,16-tetraen-7-oic acid with a conjugated 1,3,9-trienic system.
