62722-98-9 Usage
Chemical structure
A long-chain fatty acid ester with a complex structure, composed of a 16-carbon chain, a hexadecanyl group, and an acetate group.
Functional groups
Contains a 4-methyl-2,5-dioxo-2,5-dihydrofuran-3-yl group, which adds complexity to its composition.
Molecular weight
Approximately 392.62 g/mol (calculated from the molecular formula)
Physical state
Likely a liquid or a semi-solid at room temperature, due to the long-chain structure and ester functional group.
Solubility
Expected to be soluble in organic solvents such as ethanol, methanol, and acetone, but not very soluble in water.
Applications
Potential uses in the pharmaceutical, cosmetic, and food industries, due to its possible biological activities and properties.
Further research
Additional studies and analysis are needed to fully understand the effects and potential uses of 16-(4-methyl-2,5-dioxo-2,5-dihydrofuran-3-yl)hexadecan-2-yl acetate.
Safety
The safety profile of 16-(4-methyl-2,5-dioxo-2,5-dihydrofuran-3-yl)hexadecan-2-yl acetate is not well-established, and it should be handled with caution until more information is available.
Stability
The stability of 16-(4-methyl-2,5-dioxo-2,5-dihydrofuran-3-yl)hexadecan-2-yl acetate under various conditions (e.g., temperature, pH, light exposure) is not well-known and would require further investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 62722-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,2 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62722-98:
(7*6)+(6*2)+(5*7)+(4*2)+(3*2)+(2*9)+(1*8)=129
129 % 10 = 9
So 62722-98-9 is a valid CAS Registry Number.
62722-98-9Relevant academic research and scientific papers
A facile synthesis and enzymatic resolution of naturally occurring remotely functionalized alkylmethylmaleic anhydrides from Aspergillus wentii: Aspergillus acids A-D
Easwar, Srinivasan,Argade, Narshinha P.
, p. 831 - 838 (2007/10/03)
The first synthesis of four new naturally occurring remotely functionalized secondary mould metabolite anhydrides 1a-d is described starting from N-p-tolyl citraconimide (5) in three to six steps and 20-65% overall yields. The condensation of triphenylphosphine-maleimide adduct 6 with aldehyde 4 furnished the exoimide 7, which after isomerization, hydrolysis, and acylation gave aspergillus acid A (1a) in 54% overall yield in four steps. The condensation of adduct 6 with aldehyde 15 similarly afforded the desired imide 17 in two steps. The acid-catalyzed hydrolysis of imide 17 directly furnished aspergillus acid B (1b), exposing the latent methyl ketone present as the terminal acetylene. Sodium borohydride induced chemoselective reduction of aspergillus acid B (1b) gave aspergillus acid C (1c), which upon acetic anhydride induced acylation, furnished aspergillus acid D (1d). A facile Amano PS catalyzed acylation of aspergillus acid C (1c) gave, in good yield, the desired (+)-aspergillus acid C (1e) in 70% ee and (-)-aspergillus acid D (1f) in 72% ee. In the present enzymatic reaction, the anhydride moiety presumably plays a crucial role in the substrate recognition, binding, and resolution process. Georg Thieme Verlag Stuttgart.
