70606-00-7 Usage
Description
(2R)-Tetrahydro-5-oxo-2β-furancarbaldehyde is a furan derivative with the molecular formula C6H8O3. It features a five-membered furan ring and an aldehyde functional group, making it a versatile compound in organic synthesis and chemical reactions.
Uses
Used in Organic Synthesis:
(2R)-Tetrahydro-5-oxo-2β-furancarbaldehyde is used as a building block in organic synthesis for creating a variety of complex organic molecules. Its unique structure and functional groups allow for multiple reaction pathways, facilitating the synthesis of diverse chemical compounds.
Used in Pharmaceutical Industry:
(2R)-Tetrahydro-5-oxo-2β-furancarbaldehyde is used as an intermediate in the development of pharmaceuticals. Its reactivity and functional groups make it a valuable component in the synthesis of drug candidates, potentially leading to new treatments and therapies.
Used in Agrochemicals:
(2R)-Tetrahydro-5-oxo-2β-furancarbaldehyde is used as a reagent in the production of agrochemicals. Its chemical properties and reactivity contribute to the development of effective pesticides, herbicides, and other agricultural products.
Used in Chemical Research:
(2R)-Tetrahydro-5-oxo-2β-furancarbaldehyde is used as a subject of study in chemical research. Its unique structure and properties make it an interesting compound for scientists and researchers working in the field of organic chemistry and chemical synthesis, potentially leading to new discoveries and advancements in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 70606-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,0 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70606-00:
(7*7)+(6*0)+(5*6)+(4*0)+(3*6)+(2*0)+(1*0)=97
97 % 10 = 7
So 70606-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H6O3/c6-3-4-1-2-5(7)8-4/h3-4H,1-2H2
70606-00-7Relevant articles and documents
Unexpected stereochemistry in the lithium salt catalyzed ring expansion of nonracemic oxaspiropentanes. Formal syntheses of (-)-(4R,5R)-muricatacin and the pheromone (R)-japonilure
Bernard, Angela M.,Frongia, Angelo,Piras, Pier P.,Secci, Francesco
, p. 2923 - 2926 (2003)
(Matrix presented) The stereochemistry of the cyclobutanones 3, obtained by lithium salt catalyzed ring expansion of the optically pure oxaspiropentanes 2, depends not only on the lithium salt but also on the stereochemistry of 2. They constitute the starting material for the syntheses of the acetogenin (-)-(4R, SR)-muricatacin and the pheromone (R)-japonilure.
Preparation of novel synthons, uniquely functionalized tetrahydrofuran and tetrahydropyran derivatives
Nakada, Masahisa,Takano, Masashi,Iwata, Yukitaka
, p. 1581 - 1585 (2007/10/03)
The dianion of the acetoacetic ester reacts with epibromohydrin derivatives to afford a mixture of (Z)-2-alkoxycarbonylmethylidenetetrahydrofuran derivative and (E)-2-alkoxycarbonylmethylidenetetrahydropyran derivative. The selective formation of the tetr
MICROBIAL TRANSFORMATION OF (-)-VERNOLIC ACID INTO (4R,5R)-5-HYDROXY-γ-DECALACTONE
Albrecht, Wolfgang,Tressl, Roland
, p. 1391 - 1396 (2007/10/02)
(-)-Vernolic acid, isolated and purified from seeds of Euphorbia lagascae was administered to cultures of Sporobolomyces odorus. (4R,5R)-5-Hydroxy-γ-decalactone 1 accumulated as the main product.The configuration of the product was determined by synthesis of all four stereoisomers and comparison of spectroscopic and chromatographic data.
