476-53-9 Usage
Uses
Used in Pharmaceutical Industry:
2,8-Dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ester is used as a pharmaceutical agent for its potential therapeutic properties. Its unique structure and functional groups may contribute to its bioactivity, making it a promising candidate for the development of new drugs and treatments.
Used in Antimicrobial Applications:
This xanthene derivative can be employed as an antimicrobial agent, given its ability to target and inhibit the growth of various microorganisms. Its presence in Aspergillus sydowii suggests that it may have a role in the fungus's natural defense mechanisms against other competing microorganisms.
Used in Antioxidant Formulations:
Due to its chemical structure, 2,8-Dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ester may possess antioxidant properties, which can be utilized in various formulations to protect against oxidative stress and related diseases.
Used in Cosmetic Industry:
2,8-Dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ester's potential antimicrobial and antioxidant properties make it a suitable candidate for use in the cosmetic industry, where it can be incorporated into skincare products to promote skin health and protect against environmental damage.
Check Digit Verification of cas no
The CAS Registry Mumber 476-53-9 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 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 476-53:
(5*4)+(4*7)+(3*6)+(2*5)+(1*3)=79
79 % 10 = 9
So 476-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O6/c1-7-5-9(18)12-11(6-7)22-10-4-3-8(17)13(16(20)21-2)14(10)15(12)19/h3-6,17-18H,1-2H3
476-53-9Relevant academic research and scientific papers
The Chemistry of Fungi. Part 80. The X-Ray Crystallographic Structure of 8aβ-Bromo-5aα,5,6,7,8,8a-hexahydro-1,7α-dyhydroxy-8α-methoxycarbonylxanthone Monohydrate, a Rearrangement Product of Methyl 2α-Bromo-2β-(2,6-dimethoxybenzoyl)-7-oxabicyclohept
Ferguson, George,Kaitner, Branko,Gilmore, Jeremy,Omuaru, Victor O. T.,Whalley, W. Basil
, p. 1343 - 1348 (2007/10/02)
Treatment of methyl 2α-bromo-2β-(2,6-dimethoxybenzoyl)-7-oxabicycloheptane-3β-carboxylate (1; R1=H, R2=Br) with boron trichloride gives 8aβ-bromo-5aα-5,6,7,8,8a-hexahydro-1,7α-dihydroxy-8α-methoxycarbonylxanthone (4; R=H), as