7093-88-1

Usage

Uses

Used in Pharmaceutical Industry:
2,5-dihydrofuran-2,5-diyl diacetate is used as a synthetic intermediate for the production of various pharmaceuticals. Its role in the synthesis process is crucial for creating a range of medicinal compounds, contributing to the development of new drugs and treatments.
Used in Agrochemical Industry:
In the agrochemical sector, 2,5-dihydrofuran-2,5-diyl diacetate serves as an intermediate in the synthesis of agrochemicals. Its involvement in the production of these compounds helps in the development of effective pesticides, herbicides, and other agricultural products that are essential for crop protection and yield enhancement.
Used in Flavor and Fragrance Industry:
2,5-dihydrofuran-2,5-diyl diacetate is used as a flavoring agent and fragrance component due to its unique aroma and taste properties. Its incorporation into various products adds a distinct sensory experience, making it a valuable addition to the flavor and fragrance industry.
Used in Chemical Reactions:
As a solvent or reagent, 2,5-dihydrofuran-2,5-diyl diacetate is employed in a variety of chemical reactions. Its versatility in these processes allows for the synthesis of a wide range of organic compounds, further expanding its utility in the chemical industry.
Safety Considerations:
It is important to handle 2,5-dihydrofuran-2,5-diyl diacetate with caution, as it is potentially hazardous. Proper safety protocols should be followed to ensure the safe use and handling of 2,5-dihydrofuran-2,5-diyl diacetate in all applications.

Upstream product

• 110-00-9 furan 
• 64-19-7 acetic acid 
• 108-24-7 acetic anhydride 
• 546-67-8 lead(IV) tetraacetate 
• 3240-34-4 [bis(acetoxy)iodo]benzene 

Downstream Products

• 289-80-5 1,2-diazine 
• 82906-24-9 Acetic acid (3R,3aS,4R,6S,6aR)-6-acetoxy-3-benzoyl-2-phenyl-hexahydro-furo[3,4-d]isoxazol-4-yl ester 
• 82906-24-9 Acetic acid (3S,3aS,4R,6S,6aR)-6-acetoxy-3-benzoyl-2-phenyl-hexahydro-furo[3,4-d]isoxazol-4-yl ester 
• 497-23-4 2-buten-4-olide 
• 100-83-4 meta-hydroxybenzaldehyde 

Relevant academic research and scientific papers

FACILE SYNTHESIS OF 4-SUBSTITUTED BUTENOLIDES FROM FURAN

A variety of 4-substituted butenolides were prepared utilizing 2-acetoxyfuran as a key intermediate which can easily synthesized by anodic oxidation of furan.

Regioselective vicinal functionalization of unactivated alkenes with sulfonium iodate(i) reagents under metal-free conditions

Metal-free, molecular iodine-free direct 1,2-difunctionalization of unactivated alkenes has been reported. The sulfonium iodate(i) reagent efficiently promoted the intermolecular vicinal iodo-functionalization of a diverse range of olefins in a stereo and regioselective manner. This method enables the divergent and straightforward preparation of synthetically useful functionalities; β-iodocarboxylates, β-iodohydrins, and β-iodoethers in a one-step process. Further interconversion of iodo-functionalized derivatives allows easy access to valuable synthetic intermediates en route to biologically active molecules.

A Facile Route to 3a,8a-Dihydrofurobenzofurans.

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

2,5-diacyloxy-2,5-dihydrofuran activators for inorganic per compounds

2,5-diacyloxy-2,5-dihydrofurans corresponding to formula (I) STR1 wherein R is a C1 -C8 alkyl radical or a phenyl radical are useful as activators for inorganic per compounds in oxidizing, cleaning or disinfecting solutions.

The Regiospecific Synthesis of an Anthraquinone Based upon the Elaboration of the Adduct of 1-Acetoxyisobenzofuran with p-Benzoquinone Monoacetal

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