14400-67-0 Usage
Description
2,5-Dimethyl-3(2H)-furanone is an organic compound that is known for its distinct caramel-like aroma and fruity ester notes. It is a yellow clear liquid with a high-strength odor, making it a popular choice in the flavor and fragrance industry. 2,5-Dimethyl-3(2H)-furanone is commonly found in various natural sources such as bread, coffee, and mango, contributing to their characteristic flavors.
Uses
Used in Flavor Industry:
2,5-Dimethyl-3(2H)-furanone is used as a flavoring agent for its caramellic type aroma. It is particularly effective in enhancing the taste of various food products, such as baked goods, confectionery, and beverages, by adding a rich, sweet, and complex flavor profile.
Used in Fragrance Industry:
In the fragrance industry, 2,5-Dimethyl-3(2H)-furanone is used as a fixative agent to help stabilize and prolong the scent of perfumes and other fragrance products. Its fruity ester notes add a pleasant and versatile aroma, making it suitable for a wide range of fragrance applications.
Used in Aromatherapy:
Due to its high strength odor and pleasant aroma, 2,5-Dimethyl-3(2H)-furanone can be used in aromatherapy as a component in essential oil blends. It may help create a relaxing and comforting atmosphere, promoting a sense of well-being and reducing stress.
Check Digit Verification of cas no
The CAS Registry Mumber 14400-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14400-67:
(7*1)+(6*4)+(5*4)+(4*0)+(3*0)+(2*6)+(1*7)=70
70 % 10 = 0
So 14400-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O2/c1-4-3-6(7)5(2)8-4/h3,5H,1-2H3/t5-/m1/s1
14400-67-0Relevant articles and documents
A NEW REACTION OF ACETYLENES, THE ADDITION OF METHANOL TO 5-HYDROXYHEX-3-YN-2-ONE. SYNTHESIS OF THE "ONION FURANONE", 2-HEXYL-5-METHYL-3-FURANONE.
Thomas, Alan F.,Damm, Hanne
, p. 505 - 506 (1986)
The conversion of alkyl-substituted 4-hydroxybut-2-ynones to 2,5-dialkyl-3-furanones via 2,5-dialkyl-methoxyfurans is described.
An Unusual Substitution Reaction in a Benzotetrazine Derivative
Almerico, A. M.,Boulton, A. J.
, p. 204 - 205 (1985)
1-Methyl-3H-pyrazolobenzotetrazin-3-one decomposes in alcohols, with loss of nitrogen and intramolecular hydrogen transfer, to form 5-alkoxymethyl-1,2-dihydro-1-phenyl-3H-pyrazol-3-ones.
New 5-(2-ethenylsubstituted)-3(2H)-furanones with in vitro antiproliferative activity
Chimichi, Stefano,Boccalini, Marco,Cosimelli, Barbara,Dall'Acqua, Francesco,Viola, Giampietro
, p. 5215 - 5223 (2007/10/03)
A convenient route to new 3(2H)-furanones is described through hydrogenolysis and subsequent acidic hydrolysis of isoxazoles. The antiproliferative activity of title compounds were evaluated against leukemia-, carcinoma-, neuroblastoma-, and sarcoma-derived human cell lines in comparison to the natural compound geiparvarin. The structure activity relationship indicated that the maximum in vitro antiproliferative activity correlates with the presence of a heterocyclic ring on the ethenyl moiety.