828263-44-1 Usage
Molecular structure
2(3H)-Furanone,5-[(1S)-1-(acetyloxy)-3-methylbutyl]dihydro-4-methyl-,(4S,5R)-(9CI) has a complex molecular structure with a furan ring and an acetyloxy group.
Furanone class
It belongs to the furanone class of organic compounds, which are known for their diverse biological activities and potential applications.
Furan ring
The compound contains a furan ring, which is a five-membered heterocyclic ring with one oxygen atom.
Acetyloxy group
It has an acetyloxy group (-OAc), which is an ester functional group derived from acetic acid.
Dihydro-4-methyl substituent
The compound includes a dihydro-4-methyl group, which is a saturated hydrocarbon group with a total of six carbon atoms and a methyl group (-CH3) attached to the fourth carbon.
1S-1-(acetyloxy)-3-methylbutyl substituent
It also contains a 1S-1-(acetyloxy)-3-methylbutyl group, which is a chiral substituent with a 3-methylbutyl chain and an acetyloxy group at the first carbon.
Chiral compound
The compound is chiral, meaning it has a (4S,5R) configuration, which refers to the spatial arrangement of atoms in the molecule. Chiral compounds can have different properties and effects depending on their stereochemistry.
Potential applications
Due to its unique structure and properties, 2(3H)-Furanone,5-[(1S)-1-(acetyloxy)-3-methylbutyl]dihydro-4-methyl-,(4S,5R)-(9CI) may have potential applications in various industries, such as pharmaceuticals, fragrances, and flavorings.
Further research
More research and testing may be needed to fully understand the potential uses and effects of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 828263-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,2,6 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 828263-44:
(8*8)+(7*2)+(6*8)+(5*2)+(4*6)+(3*3)+(2*4)+(1*4)=181
181 % 10 = 1
So 828263-44-1 is a valid CAS Registry Number.
828263-44-1Relevant academic research and scientific papers
Olejniczak, Teresa,Ciunik, Zbigniew
, p. 3743 - 3749 (2004)
Both enantiomers of 5-(1′-acetoxy-3′-methylbutyl)-4,4-dimethyl- tetrahydrofuran-2-one 1a have been prepared with high enantioselectivity by microbial resolution using cultures of Fusarium solani and F. tricinctum. Enantioselectivity of lipolitic activity of F. solani and F. tricinctum was tested on four homologues of δ-acetoxy-γ-lactones (±)-1b-e. Absolute configurations of the products were determined by spectroscopic methods (1H NMR and CD) and an X-ray diffraction study.
