110793-80-1 Usage
Description
(5R)-5-but-3-en-1-yldihydrofuran-2(3H)-one, a chemical compound with the molecular formula C7H10O2, belongs to the butenolide class of organic compounds. It features a five-membered lactone ring with a double bond and possesses a chiral center, existing as a pair of enantiomers. (5R)-5-but-3-en-1-yldihydrofuran-2(3H)-one is known for its fruity and caramel-like aroma, making it a popular choice in the flavor and fragrance industry. Moreover, it serves as a precursor in organic synthesis and has demonstrated potential anti-inflammatory and anticancer properties, which are being explored for future pharmaceutical applications.
Uses
Used in Flavor and Fragrance Industry:
(5R)-5-but-3-en-1-yldihydrofuran-2(3H)-one is used as a flavoring agent for providing a fruity and caramel-like aroma in the food industry. Its unique scent profile makes it a valuable addition to various food products, enhancing their taste and appeal.
Used in Fragrance Production:
In the fragrance industry, (5R)-5-but-3-en-1-yldihydrofuran-2(3H)-one is used as a key component to create complex and pleasant scents for perfumes, cosmetics, and other scented products. Its ability to contribute to the overall aroma profile makes it an essential ingredient in the formulation of various fragrances.
Used in Organic Synthesis:
(5R)-5-but-3-en-1-yldihydrofuran-2(3H)-one serves as a precursor in organic synthesis, allowing chemists to create a wide range of other chemical compounds with diverse applications. Its unique structure and reactivity make it a versatile building block for the development of new molecules with potential uses in various industries.
Used in Pharmaceutical Research:
(5R)-5-but-3-en-1-yldihydrofuran-2(3H)-one is being investigated for its potential anti-inflammatory and anticancer properties. Researchers are exploring its use as a therapeutic agent in the development of new drugs to treat various medical conditions, particularly those related to inflammation and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 110793-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,7,9 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 110793-80:
(8*1)+(7*1)+(6*0)+(5*7)+(4*9)+(3*3)+(2*8)+(1*0)=111
111 % 10 = 1
So 110793-80-1 is a valid CAS Registry Number.
110793-80-1Relevant articles and documents
Process development of halaven: Synthesis of the C14-C35 fragment via iterative nozaki-hiyama-kishi reaction-williamson ether cyclization
Austad, Brian C.,Benayoud, Farid,Calkins, Trevor L.,Campagna, Silvio,Chase, Charles E.,Choi, Hyeong-Wook,Christ, William,Costanzo, Robert,Cutter, James,Endo, Atsushi,Fang, Francis G.,Hu, Yongbo,Lewis, Bryan M.,Lewis, Michael D.,McKenna, Shawn,Noland, Thomas A.,Orr, John D.,Pesant, Marc,Schnaderbeck, Matthew J.,Wilkie, Gordon D.,Abe, Taichi,Asai, Naoki,Asai, Yumi,Kayano, Akio,Kimoto, Yuichi,Komatsu, Yuki,Kubota, Manabu,Kuroda, Hirofumi,Mizuno, Masanori,Nakamura, Taiju,Omae, Takao,Ozeki, Naoki,Suzuki, Taeko,Takigawa, Teiji,Watanabe, Tomohiro,Yoshizawa, Kazuhiro
, p. 327 - 332 (2013/04/10)
Multikilogram manufacturing process of the Halaven C14-C35 fragment is described. The synthesis features convergent assembly of subunits by iterative asymmetric Ni/Cr-mediated coupling executed in fixed equipment. Georg Thieme Verlag Stuttgart - New York.
A direct method for the conversion of terminal epoxides into γ-butanolides
Movassaghi, Mohammad,Jacobsen, Eric N.
, p. 2456 - 2457 (2007/10/03)
A new and efficient process for the conversion of terminal epoxides to γ-butanolides is described involving Lewis acid promoted epoxide ring-opening by 1-morpholino-2-trimethylsilyl acetylene. Addition of a terminal epoxide to a solution of the ynamine an
Conversion of hydroxy nitriles to lactones using Rhodococcus rhodochrous whole cells
Taylor, Stephen K.,Chmiel, Nikolas H.,Simons, Lloyd J.,Vyvyan, James R.
, p. 9084 - 9085 (2007/10/03)
-
