7093-88-1 Usage
General Description
2,5-dihydrofuran-2,5-diyl diacetate is a chemical compound with the molecular formula C8H10O4. It is a diester composed of an organic molecule known as furan, which consists of a five-membered ring containing four carbon atoms and one oxygen atom. The compound is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It can also be employed as a solvent or reagent in various chemical reactions. 2,5-dihydrofuran-2,5-diyl diacetate may also have applications in the flavor and fragrance industry due to its unique aroma and taste properties. However, it is important to handle this compound with caution, as it is potentially hazardous and should be used in accordance with proper safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 7093-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,9 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7093-88:
(6*7)+(5*0)+(4*9)+(3*3)+(2*8)+(1*8)=111
111 % 10 = 1
So 7093-88-1 is a valid CAS Registry Number.
7093-88-1Relevant articles and documents
FACILE SYNTHESIS OF 4-SUBSTITUTED BUTENOLIDES FROM FURAN
Shono, Tatsuya,Matsumura, Yoshihiro,Yamane, Shin-ichiro
, p. 3269 - 3272 (1981)
A variety of 4-substituted butenolides were prepared utilizing 2-acetoxyfuran as a key intermediate which can easily synthesized by anodic oxidation of furan.
A Facile Route to 3a,8a-Dihydrofurobenzofurans.
Holzapfel, Cedric W.,Williams, D. Bradley G.
, p. 8555 - 8564 (2007/10/02)
Consecutive employment of palladium-catalysis and samarium(II)iodide-induced radical chemistry allows access to analogues of the ABC enol ether tricycle of aflatoxin B1 (1).The Pd-assisted coupling of tributylstannyl ethers of various 2-iodophenols with 2
The Regiospecific Synthesis of an Anthraquinone Based upon the Elaboration of the Adduct of 1-Acetoxyisobenzofuran with p-Benzoquinone Monoacetal
Russell, Richard A.,Evans, David A. C.,Warrener, Ronald N.
, p. 1699 - 1707 (2007/10/02)
1-Acetoxyisobenzofuran (4) reacts regiospecifically with 4,4-dimethoxycyclohexa-2,5-dienone (p-benzoquinone monoacetal) (6) to yield a single cycloadduct with endo stereochemistry.Treatment of this adduct (7) with sodium methoxide formed 1,10-di
