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3-(benzoyloxy)-2-methyl-4H-pyran-4-one is a chemical compound belonging to the pyranone family, characterized by a molecular formula of C15H12O4. It features a benzoyloxy group attached to the third carbon of the pyran ring, which endows it with unique chemical properties and reactivity.

6151-06-0

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6151-06-0 Usage

Uses

Used in Organic Synthesis:
3-(benzoyloxy)-2-methyl-4H-pyran-4-one is utilized as a building block in organic synthesis, providing a versatile starting point for the creation of various complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-(benzoyloxy)-2-methyl-4H-pyran-4-one is employed as a key intermediate for the development of new drugs, leveraging its potential therapeutic properties.
Used in Drug Development:
3-(benzoyloxy)-2-methyl-4H-pyran-4-one is used in the development of new drugs due to its potential anti-inflammatory and antioxidant effects, which may contribute to the treatment of various diseases and conditions.
Used in Material Science:
Due to its unique chemical structure, 3-(benzoyloxy)-2-methyl-4H-pyran-4-one may also find applications in the development of new materials, where its reactivity and properties can be harnessed for specific uses in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6151-06-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6151-06:
(6*6)+(5*1)+(4*5)+(3*1)+(2*0)+(1*6)=70
70 % 10 = 0
So 6151-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C24H20N4O2S2/c1-30-17-12-10-16(11-13-17)27-21(29)20-18-8-5-9-19(18)32-22(20)28-23(27)25-26-24(28)31-14-15-6-3-2-4-7-15/h2-4,6-7,10-13H,5,8-9,14H2,1H3

6151-06-0Upstream product

6151-06-0Downstream Products

6151-06-0Relevant academic research and scientific papers

Process for the manufacture of γ-pyrones

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, (2008/06/13)

A process for the manufacture of 3-hydroxy-2-alkyl-4-pyrones of formula I is provided. STR1 The process comprises cyclizing a compound of formula II, STR2 in acidic medium and hydrolyzing the ester formed thereby to produce compound I. R1 represents methyl or ethyl; R2 represents lower alkanoyl or optionally substituted benzoyl; R3 represents --OH or --NR4 R5 ; and, R4 and R5 may be alike or different and represent lower alkyl. The pyrones of formula I wherein R1 represents methyl or ethyl are known flavorants and odorants.

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