3566-57-2 Usage
Uses
Used in Flavor and Fragrance Industry:
3,4-Dihydroxy-5-Methyl-2-Furanone is used as a flavoring agent for its sweet, fruity, and strawberry-like aroma. It is particularly popular in the formulation of strawberry flavors due to its potent fragrance, which allows for its use in low concentrations.
Used in Food Industry:
3,4-Dihydroxy-5-Methyl-2-Furanone is used as a flavor enhancer in various food products, providing a natural and pleasant strawberry-like taste. Its strong aroma makes it an effective ingredient in food formulations, even when used in small amounts.
Used in Cosmetics and Personal Care Products:
3,4-Dihydroxy-5-Methyl-2-Furanone is used as a fragrance ingredient in cosmetics and personal care products, such as perfumes, lotions, and soaps. Its sweet and fruity aroma adds a pleasant scent to these products, enhancing the overall sensory experience for the user.
Used in Aromatherapy:
3,4-Dihydroxy-5-Methyl-2-Furanone can be used in aromatherapy applications for its calming and uplifting effects. Its sweet and fruity aroma can help create a relaxing atmosphere and promote a sense of well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 3566-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3566-57:
(6*3)+(5*5)+(4*6)+(3*6)+(2*5)+(1*7)=102
102 % 10 = 2
So 3566-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H6O4/c1-2-3(6)4(7)5(8)9-2/h2,7-8H,1H3
3566-57-2Relevant academic research and scientific papers
Method for resolving racemic mixtures of 5-substituted 4-hydroxy-2-furanones
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, (2008/06/13)
This invention affords a solution to the technical problem of obtaining one or both enantiomers of 5-substituted 4-hydroxyfuran-2-ones in pure form by resolution with enantiomerically pure bases. Racemic mixtures of 5-substituted 4-hydroxy-2(5H)-furanones, including 5-substituted and 5,5-disubstituted, 4-hydroxy and 3,4-dihydroxy furanones are separated into pure enantiomers by crystallization with an enantiomerically pure base, such as cinchonidine. In specific solvent mixtures, for example, 95% ethanol, the diastereomerically pure salt of one enantiomer crystallizes. The enantiomerically pure furanone can then be obtained simply by filtration and treatment of the salt with an acid, for example, trifluoracetic acid, followed by precipitation with water, filtration and drying. Moreover, the other enantiomer may be equally obtained in pure form by evaporation of the mother liquor, followed by the same treatment of the salt as described before.
