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2-Methyl-4,5,6,7-tetrafluorobenzo[b]furan is a synthetic organic compound characterized by its unique molecular structure. It features a benzofuran ring system, which is a fusion of a benzene ring with a furan ring. The molecule is further distinguished by the presence of a methyl group at the 2-position and four fluorine atoms at the 4, 5, 6, and 7-positions. This chemical is known for its potential applications in various industrial sectors, including pharmaceuticals and materials science, due to its specific electronic and steric properties. The fluorination pattern can influence its reactivity, stability, and interaction with other molecules, making it a subject of interest for chemical research and development.

3265-75-6

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3265-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3265-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3265-75:
(6*3)+(5*2)+(4*6)+(3*5)+(2*7)+(1*5)=86
86 % 10 = 6
So 3265-75-6 is a valid CAS Registry Number.

3265-75-6Downstream Products

3265-75-6Relevant academic research and scientific papers

Partially Fluorinated Heterocyclic Compounds. Part 16. Preparation of Furan Derivatives from Pentafluorophenyl and Heptafluoro-2-naphthyl Prop-2-ynyl Ethers with Aromatic Compounds, and the Isolation of Hydrogen-abstraction Products

Brooke, Gerald M.

, p. 107 - 110 (2007/10/02)

Pentafluorophenyl and heptafluoro-2-naphthyl prop-2-ynyl ethers react in N,N-diethylaniline to give among other products 2-methylfuran derivatives formed by hydrogen-abstraction reactions, and 2-(diethylaminobenzyl)furan derivatives ; the 2-fluoromethylfuran (16) is also formed from (5).No aromatic substitution products are obtained from (5) with nitrobenzene or benzylidyne trifluoride.It was not possible to distinguish between homolytic and heterolytic fission of the aliphatic C-F bonds in the Claisen rearrangement intermediates (8) and (9) involved in these reactions.

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