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1,2,3-trichloro-3,4,4-trifluorocyclobutene is a halogenated cyclobutene compound characterized by the presence of three chlorine atoms and three fluorine atoms. This organic molecule features a four-membered carbon ring with a double bond, and the halogen atoms are attached to different carbon atoms, resulting in a unique structure. Due to its halogenated nature, 1,2,3-trichloro-3,4,4-trifluorocyclobutene may exhibit properties such as increased stability, reactivity, and potential applications in various chemical processes. However, it is essential to consider the potential environmental and health risks associated with halogenated compounds, as they can be persistent and toxic. Further research and analysis are required to fully understand the properties, applications, and potential hazards of 1,2,3-trichloro-3,4,4-trifluorocyclobutene.

3762-49-0

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3762-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3762-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3762-49:
(6*3)+(5*7)+(4*6)+(3*2)+(2*4)+(1*9)=100
100 % 10 = 0
So 3762-49-0 is a valid CAS Registry Number.

3762-49-0Upstream product

3762-49-0Downstream Products

3762-49-0Relevant academic research and scientific papers

Method for gas phase catalytic synthesis of 3,4,4-trifluorocyclobutene

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Paragraph 0022; 0026-0031; 0037-0042, (2020/04/29)

The invention relates to a method for gas phase catalytic synthesis of 3,4,4-trifluorocyclobutene, and belongs to the field of organic chemical synthesis. According to the method, hexachlorobutadiene(the molecular formula is CCl2=CCl-CCl=CCl2), chlorine (the molecular formula is Cl2) and anhydrous hydrogen fluoride (the molecular formula is HF) generate 1,2,3-trichloro-3,4,4-trifluorocyclobutene(the molecular formula is Cyclo-CF2-CFCl-CCl=CCl-) in a gas phase manner under the action of a cyclofluorination catalyst; and under the action of a hydrodechlorination catalyst, the 1,2,3-trichloro-3,4,4-trifluorocyclobutene and hydrogen generate 3,4,4-trifluorocyclobutene (the molecular formula is Cyclo-CF2-CFH-CH=CH-) in a gas phase manner. According to the invention, the method has characteristics of cheap and easily-available raw materials, simple separation and purification of product and less industrial three-waste, and is suitable for industrial production.

Catalytic Gas-phase Fluorination of Hexachlorobutadiene to 1,2-Dichlorotetrafluorocyclobutene over Cr/Zn-based Catalysts

He, Jinwei,Zhang, Mengxue,Zhou, Biao,Zhou, Xiaomeng

, p. 760 - 770 (2018/02/28)

In this paper, the gas-phase fluorination of hexachlorobutadiene (HCBD) to synthesize 1,2-dichlorotetrafluorocyclobutene (DTB) was carried out over a series of Cr/M/Zn catalysts (M = Ni, Co, Cu, In, Al). The influence of prefluorination by different fluorinating agents (HF, 95%HF + 5%Cl2, 95%HF + 5%O2, CF2O, CF2Cl2) on catalytic performance of Cr/Co/Zn sample was also investigated. The addition of prompters to the Cr/Zn catalyst improved remarkably its catalytic properties. The Cr/Ni/Zn catalyst exhibited the best catalytic activity (1.318 mmol/h/g) at 390 °C and the Cr/Co/Zn catalyst showed the best DTB selectivity (42.5%) at 350 °C. Compared to that of gaseous HF, the catalytic performance of the Cr/Co/Zn catalyst after treatment by HF + O2 and CF2O increased considerably, whereas for HF + Cl2 and CF2Cl2 it showed little effect. In order to identify the different species (Cr─O, Cr─F, CrOxFy) present on catalysts’ surface and determine their exact role, these catalysts before and after the reaction were characterized by X-ray photoelectron spectroscopy. It was found that the concentration of the various species was responsible for the activity and lifetime of catalysts. Moreover, a possible reaction route is proposed based upon the product distribution. The most feasible formation pathway of DTB proceeded via the cyclization of C4Cl4F2 or C4Cl3F3 to yield c-C4Cl4F2 and c-C4Cl3F3 followed by further the Cl/F exchange.

Method for synthesizing fluorochloro succinic acid

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Paragraph 0022-0027, (2018/04/03)

The invention relates to a method for synthesizing fluorochloro succinic acid, and belongs to the field of organic chemical synthesis. The method for synthesizing fluorochloro succinic acid is characterized in that hexachlorobutadiene (the molecular formula is as follow: CCl2 being equal to CCl-CCl being equal to CCl2) generates fluorochloro cyclobutene (the molecular formula is as follow: Cyclo-C2FxCly-CCl being equal to CCl-, wherein the sum of the x and y is 4) under the effect of cyclo-fluorinated catalysts; then, the fluorochloro succinic acid (the molecular formula is HOOC-C2FxCly-COOH)is generated under the effect of oxidizing agents. CCl2 is equal to CCl-CCl being equal to CCl2 arrow Cyclo-C2FxCly-CCl being equal to CCl- arrow HOOC-C2FxCly-COOH. The method has the advantages thatthe raw materials are cheap; the resources can be conveniently obtained; the product separation and purification are simple; the industrial production is easy; three industrial wastes (waste water, waste solid and waste water) are few.

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