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5,5'-(ethane-1,2-diyl)bis(furan-2-carbaldehyde) is an organic compound with the molecular formula C12H12O4. It is a bis-furan derivative, characterized by two furan-2-carbaldehyde units connected by an ethane-1,2-diyl bridge. This chemical is known for its potential applications in the synthesis of various organic compounds and materials, such as polymers and pharmaceuticals. Its structure provides a unique platform for further chemical modifications and reactions, making it a valuable intermediate in organic chemistry.

7327-92-6

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7327-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7327-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7327-92:
(6*7)+(5*3)+(4*2)+(3*7)+(2*9)+(1*2)=106
106 % 10 = 6
So 7327-92-6 is a valid CAS Registry Number.

7327-92-6Downstream Products

7327-92-6Relevant academic research and scientific papers

Value-added chemicals from biomass-derived furans: radical functionalisations of 5-chloromethylfurfural (CMF) by metal-free ATRA reactions

Dasi, Rajesh,Schmidhuber, Daniel,Gronbach, Lisa Marie,Rehbein, Julia,Brasholz, Malte

, p. 1626 - 1631 (2021)

Biomass-derived 5-chloromethylfurfural (CMF), a congener of the well-known carbohydrate-based platform chemical 5-hydroxymethylfurfural (HMF), can efficiently be functionalised by radical transformations of its benzylic chloromethyl group. We report here the first examples of these radical reactions by way of metal-free, triethylborane/oxygen-induced atom transfer radical addition (ATRA) reactions between CMF and styrenes, which proceed with high yield and selectivity. The key intermediate, the 2-formyl-5-furfuryl radical derived from CMF, and its radical addition reactions were studied with regard to its electronic structure,i.e.spin density distribution and frontier molecular orbitals based on the NBO ansatz and activation barriers of the addition step using DFT and post-HF methods.

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