33662-58-7 Usage
Uses
Used in Pharmaceutical Industry:
METHYL 2,4-DIHYDROXY-3-METHYLBENZOATE is used as an active ingredient for its anti-inflammatory properties, particularly in topical treatments for various skin conditions.
Used in Cosmetics Industry:
METHYL 2,4-DIHYDROXY-3-METHYLBENZOATE is used as a key component in skincare products, leveraging its antioxidant properties to protect the skin and enhance its overall health.
Used in Fragrance Industry:
METHYL 2,4-DIHYDROXY-3-METHYLBENZOATE is used as a flavoring agent in food products, adding a subtle, sweet aroma to enhance the sensory experience of the product.
Used in Flavoring Industry:
METHYL 2,4-DIHYDROXY-3-METHYLBENZOATE is used as a precursor in the synthesis of other organic compounds, contributing to the development of new products and formulations in various industries.
Synthesis:
METHYL 2,4-DIHYDROXY-3-METHYLBENZOATE is typically synthesized through the esterification of 2,4-dihydroxy-3-methylbenzoic acid with methanol, resulting in a stable and aromatic compound.
Check Digit Verification of cas no
The CAS Registry Mumber 33662-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,6 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33662-58:
(7*3)+(6*3)+(5*6)+(4*6)+(3*2)+(2*5)+(1*8)=117
117 % 10 = 7
So 33662-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O4/c1-5-7(10)4-3-6(8(5)11)9(12)13-2/h3-4,10-11H,1-2H3
33662-58-7Relevant academic research and scientific papers
Synthesis of isothiochroman 2,2-dioxide and 1,2-benzooxathiin 2,2- dioxide gyrase B inhibitors
Peixoto, Christophe,Laurin, Patrick,Klich, Michel,Dupuis-Hamelin, Claudine,Mauvais, Pascale,Lassaigne, Patrice,Bonnefoy, Alain,Musicki, Branislav
, p. 1741 - 1745 (2007/10/03)
The design, synthesis and in vitro biological evaluation of isothiochroman 2,2-dioxide and 1,2-benzooxathiin 2,2-dioxide analogues of coumarin inhibitors of gyrase B are described. Compared to coumarin derivatives, compounds of the 1,2-benzooxathiin 2,2-dioxide series display improved inhibitory potency in negative supercoiling of relaxed DNA gyrase. (C) 2000 Elsevier Science Ltd.
