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2268-44-2

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2268-44-2 Usage

Description

1 1 2 2-Tetrachloro-1 3 3 3-tetrafluoropropane, commonly known as CFC-114, is a chlorofluorocarbon compound characterized by its dense, colorless, and non-flammable properties. It is not easily reactive with other chemicals, which makes it suitable for various industrial applications. However, it is also recognized as a potent greenhouse gas and an ozone-depleting substance, causing significant environmental concerns.

Uses

Used in Refrigeration Industry:
1 1 2 2-Tetrachloro-1 3 3 3-tetrafluoropropane is used as a refrigerant in the refrigeration industry due to its non-flammable and non-reactive nature, providing a safe and efficient means of cooling.
Used in Industrial Solvents:
In the chemical industry, 1 1 2 2-Tetrachloro-1 3 3 3-tetrafluoropropane serves as a solvent for various applications, taking advantage of its stability and non-reactivity with other chemicals.
Environmental Considerations:
Despite its utility, the use of CFC-114 has been regulated under the Montreal Protocol due to its classification as a potent greenhouse gas and an ozone-depleting substance. Efforts are underway to phase out its production and use to minimize its adverse effects on the environment. Alternatives are being sought to replace CFC-114 in both refrigeration and industrial solvent applications to ensure environmental sustainability.

Check Digit Verification of cas no

The CAS Registry Mumber 2268-44-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2268-44:
(6*2)+(5*2)+(4*6)+(3*8)+(2*4)+(1*4)=82
82 % 10 = 2
So 2268-44-2 is a valid CAS Registry Number.

2268-44-2Relevant articles and documents

Copper-Substituted Chromium Oxide Compositions, Their Preparation, and Their Use as Catalysts and Catalyst Precursors

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Page/Page column 12, (2010/06/22)

A crystalline alpha-chromium oxide where from about 0.05 atom % to about 5 atom % of the chromium atoms in the alpha-chromium oxide lattice are replaced by divalent copper (Cu+2) atoms is disclosed. Also disclosed is a chromium-containing catalyst composition comprising as a chromium-containing component the crystalline copper-substituted alpha-chromium oxide; and methods for preparing a composition comprising the crystalline copper-substituted alpha-chromium oxide. One method involves (a) co-precipitating a solid by adding ammonium hydroxide to an aqueous solution of a soluble copper salt and a soluble trivalent chromium salt that contains at least three moles of nitrate per mole of chromium in the solution and has a copper concentration of from about 0.05 atom % to about 5 atom % of the total concentration of copper and chromium in the solution; and after at least three moles of ammonium per mole of chromium in the solution has been added to the solution, (b) collecting the co-precipitated solid formed in (a); (c) drying the collected solid; and (d) calcining the dried solid. Another method involves (a) preparing an aqueous solution of a soluble copper salt and a soluble trivalent chromium salt that contains a copper concentration of from about 0.05 atom % to about 5 atom % of the total concentration of copper and chromium in the solution, (b) evaporating the solution to dryness, and (c) calcining the dried solid. Also disclosed is a chromium-containing catalyst composition comprising a chromium-containing component prepared by treating the crystalline copper-substituted alpha-chromium oxide with a fluorinating agent; and a process for changing the fluorine distribution (i.e., content and/or arrangement) in a hydrocarbon or halogenated hydrocarbon in the presence of a catalyst. The process involves using as the catalyst a composition comprising the crystalline copper-substituted alpha-chromium oxide and/or the treated copper-substituted alpha-chromium oxide.

Preparation of composition containing chromium, oxygen, and either silver or palladium, and their use as catalysts and catalyst precursors

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Page/Page column 8-9, (2008/12/08)

A method for preparing a catalyst composition suitable for increasing the fluorine content in a hydrocarbon or a halogenated hydrocarbon is disclosed. The method involves (a) co-precipitating a solid by adding ammonium hydroxide to an aqueous solution of a soluble trivalent chromium salt and a soluble salt of a modifier metal selected from silver and palladium, that contains at least three moles of nitrate (i.e., NO3?) per mole of chromium (i.e., Cr+3) in the solution and has a modifier metal concentration of from about 0.05 atom % to about 10 atom % of the total concentration of modifier metal and chromium in the solution to form an aqueous mixture containing co-precipitated solid and dissolved ammonium nitrate; and after at least three moles of ammonium hydroxide per mole of chromium in the solution has been added to the solution, (b) drying said aqueous mixture formed in (a); and (c) calcining the dried solid formed in (b) in an atmosphere containing at least 10% oxygen by volume (e.g., air). Also disclosed is a catalyst composition comprising alpha-chromium oxide and a modifier metal selected from silver and palladium prepared by the above method. Also disclosed is a process for increasing the fluorine content in a hydrocarbon or halogenated hydrocarbon in the presence of a catalyst; and processes using a catalyst composition comprising chromium, oxygen and a modifier metal selected from siver and palladium as essential constituent elements (e.g., a catalyst composition prepared by the above process). An azeotropic composition involving CF3CCl═CF2 and HF is also disclosed.

Thermal chlorofluorination of propyne and propadiene

Belter, Randolph K.

, p. 1611 - 1615 (2008/09/18)

Propyne and propadiene have been found to readily undergo vapor phase catalyzed chlorofluorination. At temperatures to 285 °C, the reaction forms mixtures of C3F4Cl4 isomers that differ in composition from mixtures obtained from either propane or propene.

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