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Difluoromethyl-isopropyl ether, also known as 1,1-difluoro-2-methoxypropane, is an organic compound with the chemical formula C4H8F2O. It is a colorless, volatile liquid that is soluble in organic solvents and has a molecular weight of 114.11 g/mol. This ether derivative is characterized by the presence of two fluorine atoms attached to a methyl group, which is connected to an isopropyl group through an oxygen atom. Difluoromethyl-isopropyl ether is used as a solvent and a reagent in various chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals. It is also employed in the production of fluorinated compounds due to its unique reactivity and stability. The compound is synthesized through the reaction of isopropyl alcohol with difluoromethyl chloride, and it is known for its low toxicity and environmental friendliness compared to some other fluorinated solvents.

372-13-4

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372-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 372-13-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 372-13:
(5*3)+(4*7)+(3*2)+(2*1)+(1*3)=54
54 % 10 = 4
So 372-13-4 is a valid CAS Registry Number.

372-13-4Downstream Products

372-13-4Relevant academic research and scientific papers

A SIMPLE CONVENIENT METHOD FOR PREPARATION OF DIFLUOROMETHYL ETHERS USING FLUOROSULFONYLDIFLUOROACETIC ACID AS A DIFLUOROCARBENE PRECURSOR

Chen, Qing-Yun,Wu, Sheng-Wen

, p. 433 - 440 (1989)

In the presence of catalytic amounts of sodium sulfate or cuprous iodide, a variety of alkyl and aryl difluoromethyl ethers were synthesized in moderate yields by the reaction of the corresponding alcohols and phenols with fluorosulfonyldifluoroacetic acid (1) in acetonitrile under mild conditions.Fluorosulfonyldifluoroacetate anion (5) is believed to readily eliminate SO2, CO2 and F(1-), thus liberating CF2:; insertion of difluorocarbene into O-H bonds and its capture by fluorode ion then result in the formation of ethers and by-product CF3H, respectively.

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