479-16-3 Usage
Description
4-[(3-Chloro-5-formyl-4,6-dihydroxy-2-methylbenzoyl)oxy]-2-hydroxy-3,6-dimethylbenzoic acid methyl ester is a complex organic compound characterized by its unique chemical structure. It is derived from the Evernia prunastri plant and exhibits a variety of biological activities, making it a promising candidate for various applications in the pharmaceutical and chemical industries.
Uses
Used in Antioxidant Applications:
4-[(3-Chloro-5-formyl-4,6-dihydroxy-2-methylbenzoyl)oxy]-2-hydroxy-3,6-dimethylbenzoic acid methyl ester is used as an antioxidant agent for its ability to neutralize free radicals and protect cells from oxidative damage. This property makes it a valuable component in the development of pharmaceuticals and nutraceuticals aimed at promoting overall health and preventing age-related diseases.
Used in Antimicrobial Applications:
In the pharmaceutical industry, 4-[(3-Chloro-5-formyl-4,6-dihydroxy-2-methylbenzoyl)oxy]-2-hydroxy-3,6-dimethylbenzoic acid methyl ester is used as an antimicrobial agent due to its ability to inhibit the growth of harmful microorganisms. This application can be particularly useful in the development of new antibiotics and antifungal agents to combat drug-resistant infections.
Used in Anticancer Applications:
4-[(3-Chloro-5-formyl-4,6-dihydroxy-2-methylbenzoyl)oxy]-2-hydroxy-3,6-dimethylbenzoic acid methyl ester is used as a potential anticancer agent, as it may exhibit inhibitory effects on tumor growth and progression. Further research is needed to fully understand its mechanism of action and potential synergistic effects when combined with conventional chemotherapeutic drugs.
Used in Chemical Synthesis:
In the chemical industry, 4-[(3-Chloro-5-formyl-4,6-dihydroxy-2-methylbenzoyl)oxy]-2-hydroxy-3,6-dimethylbenzoic acid methyl ester can be used as a key intermediate in the synthesis of various complex organic compounds, including pharmaceuticals, dyes, and other specialty chemicals. Its unique structure and functional groups make it a versatile building block for the development of new molecules with diverse applications.
Used in Drug Delivery Systems:
Similar to gallotannin, 4-[(3-Chloro-5-formyl-4,6-dihydroxy-2-methylbenzoyl)oxy]-2-hydroxy-3,6-dimethylbenzoic acid methyl ester can be incorporated into novel drug delivery systems to enhance its applications and efficacy against specific targets, such as cancer cells. The development of organic and metallic nanoparticles as carriers for this compound could improve its delivery, bioavailability, and therapeutic outcomes in various medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 479-16-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 479-16:
(5*4)+(4*7)+(3*9)+(2*1)+(1*6)=83
83 % 10 = 3
So 479-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H17ClO8/c1-7-5-11(8(2)15(22)12(7)18(25)27-4)28-19(26)13-9(3)14(20)17(24)10(6-21)16(13)23/h5-6,22-24H,1-4H3
479-16-3Relevant articles and documents
Chemical constituents of the lichen, Candelaria concolor: A complete NMR and chemical degradative investigation
Dias, Daniel A.,Urban, Sylvia
scheme or table, p. 925 - 939 (2010/08/19)
A detailed chemical and spectroscopic investigation of the terrestrial lichen Candelaria concolor has yielded several lichenic metabolites belonging to the pulvinic acid series, as well as several depside derivatives including pulvinic dilactone (1), vulpinic acid (4) and calycin (5). The chemical transformation of 1 to pulvinic acid (3) is reported for the first time, as is the conversion of atranorin (6) to 5-chloroatranorin (7) and then finally to 5,5'-dichloroatranorin (8) under very mild conditions. Also presented is the complete 1D and 2D NMR assignment for compounds 1, 3, 4, 5 and 8, including partial NMR chemical shift assignments for the unstable depside (7). Previously, these metabolites had only been partially assigned by NMR spectroscopy.
