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2,4-Pentanedione, 1,3-difluoro(9CI) is a chemical compound with the formula C5H6F2O. It is a colorless liquid with a fruity odor, and is commonly used as a flavoring agent in food and beverages. It is also utilized as a building block in the synthesis of other organic compounds. The chemical is considered to have low toxicity, but prolonged exposure to high concentrations can cause irritation to the eyes, skin, and respiratory system. It is important to handle this chemical with care and follow proper safety precautions when working with it.

87498-27-9

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87498-27-9 Usage

Uses

Used in Food and Beverage Industry:
2,4-Pentanedione, 1,3-difluoro(9CI) is used as a flavoring agent for imparting a fruity aroma to food and beverages. Its pleasant odor and taste make it a popular choice in the industry.
Used in Chemical Synthesis:
2,4-Pentanedione, 1,3-difluoro(9CI) is used as a building block in the synthesis of other organic compounds. Its unique structure allows it to be a versatile component in the creation of various chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 87498-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,9 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87498-27:
(7*8)+(6*7)+(5*4)+(4*9)+(3*8)+(2*2)+(1*7)=189
189 % 10 = 9
So 87498-27-9 is a valid CAS Registry Number.

87498-27-9Upstream product

87498-27-9Downstream Products

87498-27-9Relevant academic research and scientific papers

Direct fluorination of 1,3-dicarbonyl compounds

Chambers, Richard D.,Greenhall, Martin P.,Hutchinson, John

, p. 1 - 8 (2007/10/02)

In acid media, 1,3-diketones and 1,3-keloesters can be fluorinated in high yield and often with high conversion mainly to the corresponding 2-fluoro- compounds. Diesters such as diethyl malonate do not react with fluorine under the same reaction conditions. The mechanism of these reactions has been investigated and while the identity of the electrophilic fluorinating species is uncertain, we believe that the essential features of the reaction pathway are understood. Copyright

Direct Fluorination of 1,3-Dicarbonyl Compounds

Chambers, Richard D.,Greenhall, Martin P.,Hutchinson, John

, p. 21 - 22 (2007/10/02)

1,3-Dicarbonyls, such as 1,3-diketones and 1,3-ketoesters, react directly with elemental fluorine at room temperature to give the corresponding 2-fluoro- and, in some cases, 2,2-difluoro-compounds in high yield.

Room-temperature Reactions of CsSO4F with Organic Molecules containing Heteroatoms

Stavber, Stojan,Zupan, Marko

, p. 563 - 564 (2007/10/02)

Room-temperature fluorination of pentane-2,4-dione with CsSO4F gave 3-fluoro and 1,3-difluoro derivatives, while 5,5-difluorobarbituric acid was formed in high yield in a 2 h reaction at 100 deg C; 1,3-dimethyluracil was converted in methanol via cis- and trans-5-fluoro-6-methoxy derivatives into 5-fluoro-1,3-dimethyluracil in high yield and uridine into 5-fluorouridine.

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