1575-46-8 Usage
Description
3,4-Dimethyl-2,5-dihydrofuran-2-one is an organic compound that serves as an intermediate in the synthesis of various compounds with potential applications in different industries. It is characterized by its unique chemical structure and properties, making it a valuable component in the development of new products.
Uses
Used in Pharmaceutical Industry:
3,4-Dimethyl-2,5-dihydrofuran-2-one is used as an intermediate in the synthesis of 3,4-Dimethyl-5-pentyl-2-furannonanoic Acid (D477715), an F3 furan fatty acid. 3,4-Dimethyl-2,5-dihydrofuran-2-one exhibits radical-scavenging ability and anti-inflammatory properties, making it a promising candidate for the development of new drugs and therapies in the pharmaceutical industry.
Used in Chemical Synthesis:
3,4-Dimethyl-2,5-dihydrofuran-2-one is also used as a key intermediate in the synthesis of various other compounds with potential applications in different industries. Its unique chemical structure allows for further modification and functionalization, leading to the development of new products with diverse properties and uses.
Synthesis Reference(s)
Journal of Medicinal Chemistry, 31, p. 893, 1988 DOI: 10.1021/jm00400a001
Check Digit Verification of cas no
The CAS Registry Mumber 1575-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1575-46:
(6*1)+(5*5)+(4*7)+(3*5)+(2*4)+(1*6)=88
88 % 10 = 8
So 1575-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O2/c1-4-3-8-6(7)5(4)2/h3H2,1-2H3
1575-46-8Relevant articles and documents
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Adams,Gianturco
, p. 166,169 (1957)
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Carbonylation of Aldehydes in Strong Acid. A General Synthesis of 3,4-Dialkyl-2(5H)-furanones
Woo, Edmund P.,Cheng, Frank C.W.
, p. 3706 - 3707 (1986)
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Expeditious microwave-assisted synthesis of 5-alkoxyoxazoles from α-triflyloxy esters and nitriles
Jouanno, Laurie-Anne,Sabot, Cyrille,Renard, Pierre-Yves
, p. 8549 - 8555 (2012/11/07)
A rapid and general access to diversely substituted 5-alkoxyoxazoles 2 (i.e., R1, R2 = alkyl, phenyl) from easily accessible α-triflyloxy/hydroxy esters 1 and nitriles with good yields (41-76%) is reported. The versatility of the cyc
Synthesis of hetero atom modified pyrromethenones
Bongards, Christian,Gaertner, Wolfgang
, p. 5749 - 5758 (2008/09/17)
A series of six heteroaromatic compounds, ethyl-/methyl-and dimethylfuranones, thiophenones, and cyclopentenones, was synthesized and condensed with a methyl methylpropionate substituted pyrrole, yielding the "right" half of open-chain tetrapyrroles. These compounds serve as light-inducible chromophores in the plant photoreceptor phytochrome. Three-dimensional structure analysis of the 10-oxapyrromethen-1-one 25 revealed a planar conformation, similar to the dipyrromethenone parent compound, stabilized by a hydrogen bond formed between the pyrrole proton and the furanone oxygen atom. All six pyrrole-substituted heteroaromatic derivatives 25-30 show absorbances in the visible spectrum with high molar extinction coefficients. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.