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1,1,3-Trifluorobuta-1,3-diene is a fluorinated organic compound with the molecular formula C4H3F3. It is a colorless liquid with a pungent odor and is characterized by the presence of three fluorine atoms and a conjugated diene system. This molecule is an important intermediate in the synthesis of various fluorinated compounds, particularly in the pharmaceutical and agrochemical industries. Due to its reactivity, it can undergo various chemical reactions, such as Diels-Alder reactions, which are useful for constructing complex molecular structures. The compound is also known for its potential applications in materials science, as it can be used to create new polymers with unique properties. However, it is important to handle 1,1,3-trifluorobuta-1,3-diene with care due to its potential toxicity and reactivity.

674-85-1

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674-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 674-85-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 674-85:
(5*6)+(4*7)+(3*4)+(2*8)+(1*5)=91
91 % 10 = 1
So 674-85-1 is a valid CAS Registry Number.

674-85-1Downstream Products

674-85-1Relevant academic research and scientific papers

PREPARATION OF HALOGEN AND HYDROGEN CONTAINING ALKENES OVER METAL FLUORIDE CATALYSTS

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Page/Page column 22-23, (2009/03/07)

Halogenated alkenes, especially fluorinated alkenes can be prepared from halogenated and fluorinated alkanes, respectively, by dehydrohalogenation or dehydrofluorination in the presence of a high-surface metal fluoride or oxifluoride. Preferably, trifluoroethylene, pentafluoropropene, tetrafluorobutenes or trifluorobutadiene are prepared. Aluminium fluoride is highly suitable. The metal fluoride or oxifluoride can be applied supported on a carrier.

Method for producing 4,4,4- Trifluorobutane-2-One

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Page/Page column 7, (2009/09/26)

The present invention provides a novel method for preparing 4,4,4-trifluorobutane-2-one by providing a fluorobutene selected from the group consisting of 2,4,4,4-tetrafluoro-1-butene, (E)-1,1,1,3-tetrafluoro-2-butene, (Z)-1,1,1,3-tetrafluoro-2-butene, and mixture thereof; and reacting the fluorobutene(s) with a proton acid and water.

A METHOD FOR PRODUCING 4,4,4-TRIFLUOROBUTANE-2-ONE

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Page/Page column 26; 28, (2008/06/13)

The present invention provides a novel method for preparing 4,4,4-trifluorobutane-2-one by providing a fluorobutene selected from the group consisting of 2,4,4,4-tetrafluoro-1-butene, (E)- 1,1,1,3-tetrafluoro-2-butene, (Z)-1,1,1,3-tetrafluoro-2-butene, and mixture thereof; and reacting the fluorobutene(s) with a proton acid and water.

FLUOROBUTENE DERIVATIVES AND PROCESS FOR PRODUCING SAME

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Page 22-23; 24, (2008/06/13)

The present invention provides novel compounds, 2, 4,4,4-tetrafluoro-1-butene and (E)- and (Z)-1,1,1,3-tetrafluoro-2 butenes. Furthermore, the present invention provides the following novel first and second processes for producing 2,4,4,4-tetrafluoro-1-butene, (E)- and (Z)-1,1,1,3-tetrafluoro-2-butenes, and 1,1,3-trifluorobutadiene. The first process is a process for producing 2,4,4,4-tetrafluoro-1-butene by heating 1,1,1,3,3-pentaflurobutane at from about 200°C to about 700°C. The second process is a process for producing (E)- and (Z)-1,1,1,3-tetrafluoro-2-butenes by bringing 1,1,1,3,3-pentafluorobutane with a base. By the first and second processes, it is possible to obtain respective target fluorobutenes with high selectivity. In third to fifth processes, 2,4,4,4-tetrafluoro-1-butene, (E)- and (Z)-1,1,1,3-tetrafluoro-2-butene, and 1,1,3,-trifluorobutadiene can be produced by heating 1,1,1,3,3-pentafluorobutane in the presence of a catalyst. This catalyst can be regenerated by the contact with a halogen-containing gas in sixth process.

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