1073-11-6 Usage
Description
Dihydro-5-methyl-5-vinylfuran-2(3H)-one is an organic compound with a unique structure that features a furan ring and a gamma-lactone group. It is known for its floral aroma and is found in various natural sources, including papaya, wine, tea, grapes (Vitis vinifera), coriander seed, calamus, sage, and maté. dihydro-5-methyl-5-vinylfuran-2(3H)-one serves as an intermediate in the synthesis of γ-CEHC (C249200), which is a metabolite of γ-Tocopherol (T526140), one of the naturally occurring forms of Vitamin E.
Uses
1. Used in Pharmaceutical Industry:
Dihydro-5-methyl-5-vinylfuran-2(3H)-one is used as an intermediate in the synthesis of γ-CEHC (C249200) for its role in the production of Vitamin E. Vitamin E is essential for various biological functions, including antioxidant activity and maintaining the integrity of cell membranes.
2. Used in Flavor and Fragrance Industry:
Dihydro-5-methyl-5-vinylfuran-2(3H)-one is used as a fragrance ingredient for its floral aroma. It contributes to the creation of various scents in the perfumery and cosmetics industry, enhancing the sensory experience of products.
3. Used in Food and Beverage Industry:
Dihydro-5-methyl-5-vinylfuran-2(3H)-one is used as a flavor enhancer in the food and beverage industry. Its floral aroma can be utilized to add a pleasant and distinct taste to various products, such as beverages, confectionery, and other food items.
4. Used in Nutraceutical Industry:
Dihydro-5-methyl-5-vinylfuran-2(3H)-one is used as a component in the synthesis of Vitamin E, which has various health benefits. It can be incorporated into nutraceutical products, such as dietary supplements and functional foods, to support overall health and well-being.
5. Used in Agricultural Industry:
Dihydro-5-methyl-5-vinylfuran-2(3H)-one can be used in the agricultural industry as a natural compound with potential applications in pest control or as a component in the development of biopesticides, leveraging its unique chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1073-11-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1073-11:
(6*1)+(5*0)+(4*7)+(3*3)+(2*1)+(1*1)=46
46 % 10 = 6
So 1073-11-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O2/c1-3-7(2)5-4-6(8)9-7/h3H,1,4-5H2,2H3
1073-11-6Relevant articles and documents
Stereoselective synthesis of 1-methyl-1,2-and 1,3-cyclopentanediols via γ-lactones
Niidu,Paju,Mueuerisepp,Jaerving,Kailas,Pehk,Lopp
, p. 1751 - 1760 (2013)
A method for the synthesis of 1-methylcarbapentofuranose derivatives was developed, where 1,2-cis- and 1,2-trans-4-hydroxymethyl-1- methylcyclopentanediols were obtained from intramolecular opening of a 4-epoxy-4-methyl-γ-lactone. An intramolecular aldol reaction of 4-methyl-4-(2-oxoethyl)-γ-lactone derivatives yielded 1,3-cis- and 1,3-trans-4-hydroxymethyl-1-methylcyclopentanediols.
Palladium-Catalyzed Cyclization of Free Hydroxyalkenoic Acids: Regio- and Chemoselective Access to Methylene Lactones
Mostinski, Yelena,Kotikalapudi, Ramesh,Valerio, Viviana,Nataf, Riva,Tsvelikhovsky, Dmitry
, p. 1164 - 1169 (2017)
A general and collective synthesis of medium-sized methylene lactones via controlled cyclizations of easily accessible collective precursors is described. The rapid composition of key–hydroxyalkenoic acid scaffold yields an assembly of oxocanones, oxepanones, and pyranones in a regioselective and stereodirected fashion via palladium-catalyzed cyclization. (Figure presented.).
CYCLIZATION PROCESSES OF HYDROXYALKENOIC AICDS AND PRODUCTS THEREOF
-
Page/Page column 32; 38-39, (2018/09/12)
The invention provides efficient cyclization processes of hydroxyalkenoic acids and products produced therefrom. The following reactions are claimed: Formula (I), (II), (V) and (VI).
