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1,2-difluoronaphthalene is an organic compound with the chemical formula C10H6F2. It is a halogenated derivative of naphthalene, a polycyclic aromatic hydrocarbon consisting of two fused benzene rings. The presence of two fluorine atoms at the 1 and 2 positions of the naphthalene molecule imparts unique chemical and physical properties to 1,2-difluoronaphthalene, such as increased electronegativity and reactivity compared to its parent compound. This fluorinated aromatic compound has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, due to its distinct electronic and steric effects. However, it is essential to handle 1,2-difluoronaphthalene with caution, as it may pose health and environmental risks, similar to other halogenated aromatics.

317-80-6

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317-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 317-80-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 317-80:
(5*3)+(4*1)+(3*7)+(2*8)+(1*0)=56
56 % 10 = 6
So 317-80-6 is a valid CAS Registry Number.

317-80-6Downstream Products

317-80-6Relevant academic research and scientific papers

Selective and efficient direct fluorination of polycyclic aromatic hydrocarbons using 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)

Stavber, Stojan,Zupan, Marko

, p. 1077 - 1078 (1996)

A new N-F fluorinating reagent 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Accufluor NFTh) was effectively used for selective fluorination of polycyclic aromatics. Naphthalene was site-selectively fluorinated to 1-fluoronaphthalene, phenanthrene to 9-fluorophenanthrene, and pyrene to 1-fluoropyrene. In a series of substituted naphthalenes the regioselectivity and effectiveness of fluorination depended on the position and the nature of the substituents.

Pyrolysis of cyclobutanes from styrenes, acrylonitrile and methyl acrylate and polyfluoroolefines

Weigert, F. J.

, p. 53 - 58 (1993)

The 2 + 2 cycloadduct of styrene and TFE (1) ring-expands and eliminates HF like a butadiene adduct to give 2,3-difluoronaphthalene (3).Cyclobutane 1 also cleaves to styrene and 1,1-difluorostyrene.Titania and other solid-acids accelerate the ring-expansi

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