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3,3-Difluorohexane is an organic compound with the chemical formula C6H12F2. It is a colorless, volatile liquid that belongs to the class of alkanes, specifically a hexane derivative with two fluorine atoms replacing hydrogen atoms at the 3rd carbon position. 3,3-Difluorohexane is characterized by its unique properties, such as a lower boiling point and increased reactivity compared to its non-fluorinated counterparts, due to the electronegativity of fluorine atoms. 3,3-Difluorohexane is primarily used as a solvent, a chemical intermediate in the synthesis of various fluorinated compounds, and as a precursor in the production of pharmaceuticals and agrochemicals. Its applications span across various industries, including chemical manufacturing, pharmaceuticals, and agriculture.

358-68-9

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358-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358-68-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 358-68:
(5*3)+(4*5)+(3*8)+(2*6)+(1*8)=79
79 % 10 = 9
So 358-68-9 is a valid CAS Registry Number.

358-68-9Downstream Products

358-68-9Relevant academic research and scientific papers

Poly-4-vinylpyridinium poly(hydrogen fluoride): A solid hydrogen fluoride equivalent reagent

Olah,Li,Wang,Surya Prakash

, p. 693 - 699 (2007/10/02)

Poly-4-vinylpyridinium poly(hydrogen fluoride) (PVPHF), containing 35-60% hydrogen fluoride by weight, was prepared as a solid hydrogen fluoride equivalent reagent. PVPHF with 60% hydrogen fluoride by weight was found to be a versatile fluorinating agent for the hydrofluorination and bromofluorination of alkanes and alkynes, fluorination of alcohols as well as other fluorination reactions. Low hydrogen fluoride content PVPHF (3 equivalents of hydrogen fluoride to 1 equivalent of 4-vinylpyridine unit) was also found to be an efficient reagent for bromofluorination of alkenes in the presence of 1,3-dibromo-5,5-dimethylhydrantoin. Fluorosulfonic acid-modified PVPHF showed enhanced reactivities for the fluorination of secondary alcohols.

Dialkylaminosulfur trifluorides as fluorinating agents

-

, (2008/06/13)

Dialkylaminosulfur trifluorides such as diethylaminosulfur trifluoride are useful in replacing hydroxyl group and carbonyl oxygen with fluorine in various organic compounds.

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