6049-93-0 Usage
Uses
Used in Cosmetics Industry:
2,3-Dihydroxy-5-methyl-benzoic acid is used as an antioxidant in cosmetics for its ability to protect the skin from oxidative damage, thereby promoting skin health and delaying the aging process.
Used in Pharmaceutical Industry:
2,3-Dihydroxy-5-methyl-benzoic acid is used as a therapeutic agent for its potential to inhibit the growth of cancer cells, offering a natural alternative for cancer treatment and prevention.
Used in Food Industry:
2,3-Dihydroxy-5-methyl-benzoic acid is used as a natural preservative in food products to extend their shelf life and maintain freshness by preventing oxidation and spoilage.
Used in Antioxidant Applications:
2,3-Dihydroxy-5-methyl-benzoic acid is used as an antioxidant for its ability to neutralize free radicals and protect against oxidative stress, which can lead to various diseases and health conditions.
Further research is being conducted to explore the various applications and potential benefits of 2,3-Dihydroxy-5-methyl-benzoic acid in different fields, including its use as a natural preservative in cosmetics and its potential role in drug delivery systems.
Check Digit Verification of cas no
The CAS Registry Mumber 6049-93-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6049-93:
(6*6)+(5*0)+(4*4)+(3*9)+(2*9)+(1*3)=100
100 % 10 = 0
So 6049-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O4/c1-4-2-5(8(11)12)7(10)6(9)3-4/h2-3,9-10H,1H3,(H,11,12)
6049-93-0Relevant academic research and scientific papers
Progress towards viridin: Synthesis of the pentacyclic furanosteroid ring system via o-benzoquinonoid cycloadditions
Souza, Fabio E. S.,Rodrigo, Russell
, p. 1947 - 1948 (2007/10/03)
The pentacyclic ring system of viridin is synthesised in nine steps from 4-methylguaicol by means of successive cycloadditions involving o-benzoquinonoid intermediates generated in situ.
Quassinoid Synthesis via o-Quinone Diels-Alder Reactions
Weller, Dwight D.,Stirchak, Eugene P.
, p. 4873 - 4879 (2007/10/02)
The reaction of 3,5-disubstituted o-quinones (2a, 2c) and 4-chloro-3,5-disubstituted o-quinones (2b, 2d) with simple dienes was investigated as a potential route to the quassinoid skeleton.Quinones 2a and 2c reacted in high yield at the 3,4-position with only a small excess of diene.Attempted equilibration of cis-fused cycloadducts to the trans-fused system failed due to the intervention of a stable enol form, as in 20.Compound 2c with ethyl 3,5-hexadienoate gave 15a, which upon reduction and lactonization provided BCD-ring tricyclic quassinoid analogues 18a and 19a.Again isomerization to the BC trans-fused system was not possible.The chloroquinones showed some preference for Diels-Alder reaction at the 5,6-position, but the additions were characterized generelly by low yields, side reactions, and lessened stereoselectivity.
