6121-76-2 Usage
Uses
Used in Antimicrobial Applications:
Benzoic acid, 2-heptyl-4,6-dihydroxyis used as an antimicrobial feed additive in the biogenetically modeled method of β-resorcylic acids synthesis. β-resorcylic acids are known for their potential to reduce Campylobacter colonization in broiler chickens, which is a significant concern in the poultry industry. By incorporating Benzoic acid, 2-heptyl-4,6-dihydroxy- into the feed, it can help maintain the health and well-being of the chickens, as well as improve the overall quality of the meat produced.
Used in Pharmaceutical Industry:
Benzoic acid, 2-heptyl-4,6-dihydroxymay also have potential applications in the pharmaceutical industry due to its unique chemical structure and properties. Its ability to interact with various biological molecules and pathways could make it a promising candidate for the development of new drugs or drug delivery systems. Further research and development would be required to explore these possibilities and determine the full potential of Benzoic acid, 2-heptyl-4,6-dihydroxy- in the pharmaceutical field.
Check Digit Verification of cas no
The CAS Registry Mumber 6121-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6121-76:
(6*6)+(5*1)+(4*2)+(3*1)+(2*7)+(1*6)=72
72 % 10 = 2
So 6121-76-2 is a valid CAS Registry Number.
6121-76-2Relevant academic research and scientific papers
TERT-BUTANOLYSIS OF LICHEN DEPSIDES
Huneck, Siegfried
, p. 2697 - 2698 (2007/10/02)
The scope and limit of the tert-butanolysis of 12 lichen depsides is described.Neither 2-O-methylated nor 2-O-acylated compounds are cleaved by heating with tert-butanol.Key Word Index - Depsides: tert-butanolysis.
Long-chain Phenols. Part 16. A Novel Synthesis of Homologous Orsellinic Acids and their Methyl Ethers
Durrani, Aziz A.,Tyman, John H. P.
, p. 1658 - 1666 (2007/10/02)
By the novel reaction of 3,5-dimethoxyfluorobenzene with n-alkyl-lithium compounds, followed by carbonation, homologous orsellinic acid dimethyl ethers (6-alkyl-2,4-dimethoxybenzoic acids) have been obtained.The reactions proceeded best with the homologues of methyl-lithium.These reactions are considered to occur by way of 3,5-dimethoxybenzyne. 2,4-Dimethoxyfluorobenzene did not form an aryne but gave 3-fluoro-2,6-dimethoxybenzoic acid instead.Decomposition with water of alkyl-lithium reaction mixtures from 3,5-dimethoxyfluorobenzene yielded 5-n-alkylresorcinol dimethyl ethers.Demethylaton of 6-alkyl-2,4-dimethoxybenzoic acids with boron trichloride proceeded partially and selectively to give the 6-alkyl-2-hydroxy-4-methoxybenzoic acids, and completely with aluminium chloride to give the homologous orsellinic acids.Boron tribromide was less effective, but readily gave the 5-alkyl resorcinols from the corresponding dimethyl ethers.
