425-61-6 Usage
Description
2,2,3,3-TETRAFLUORO-1,4-BUTANEDIOL, also known as Tetrafluorobutanediol, is a white crystalline powder with unique chemical properties. It is characterized by the presence of fluorine atoms in its molecular structure, which imparts specific characteristics that make it suitable for various applications.
Uses
Used in Enzymatic Synthesis:
2,2,3,3-TETRAFLUORO-1,4-BUTANEDIOL is used as a reactant in the enzymatic synthesis of silicone fluorinated aliphatic polyester amides. Its fluorinated nature contributes to the formation of these polymers, which have potential applications in various industries due to their unique properties.
Used in Chemical Industry:
In the chemical industry, 2,2,3,3-TETRAFLUORO-1,4-BUTANEDIOL is used as a building block for the synthesis of various fluorinated compounds. Its reactivity and stability make it a valuable component in the development of new materials with specific properties, such as enhanced chemical resistance or improved thermal stability.
Used in Pharmaceutical Industry:
2,2,3,3-TETRAFLUORO-1,4-BUTANEDIOL can also be utilized in the pharmaceutical industry as a starting material for the synthesis of fluorinated drugs. The introduction of fluorine atoms into drug molecules can significantly alter their pharmacokinetic and pharmacodynamic properties, potentially leading to improved drug efficacy and reduced side effects.
Used in Material Science:
In the field of material science, 2,2,3,3-TETRAFLUORO-1,4-BUTANEDIOL can be employed in the development of advanced materials with enhanced properties, such as increased hydrophobicity, improved mechanical strength, or enhanced thermal stability. These materials can find applications in various sectors, including aerospace, automotive, and electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 425-61-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 425-61:
(5*4)+(4*2)+(3*5)+(2*6)+(1*1)=56
56 % 10 = 6
So 425-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H6F4O2/c5-3(6,1-9)4(7,8)2-10/h9-10H,1-2H2
425-61-6Relevant articles and documents
Method for preparing fluorine-containing dihydric alcohol from fluorine-containing cycloolefin
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Paragraph 0007; 0034; 0037-0038, (2021/07/01)
The invention discloses a method for preparing fluorine-containing dihydric alcohol from fluorine-containing cycloolefin. The method comprises the following steps: oxidizing fluorine-containing cycloolefin serving as a raw material by using an oxidizing agent and treating the fluorine-containing cycloolefin by using a strong alkali to generate a solid mixed salt containing corresponding fluorine-containing dicarboxylate, and then generating corresponding fluorine-containing binary acyl chloride under the action of an acylating chlorination reagent; and finally, enabling the fluorine-containing binary acyl chloride and a reducing agent to be subjected to a reduction reaction under the action of a solvent and a catalyst to obtain the corresponding fluorine-containing dihydric alcohol. The specific organic solvent and catalyst are adopted, and other conditions are matched, so that the fluorine-containing cycloolefin can be effectively promoted to generate corresponding fluorine-containing dihydric alcohol with high efficiency and high yield. The method has the advantages of easily available raw materials, simple process, convenience in operation, low cost and the like, and is suitable for large-scale production of fluorine-containing dihydric alcohol.
METHOD FOR PRODUCING TETRAFLUORO COMPOUND
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Page/Page column 6, (2011/08/04)
Provided is a method for producing a tetrafluoro nitrogen-containing heterocyclic compound such as tetrafluoropyrrolidine in good yield and at low cost. The method comprises the steps of: (A) reacting a compound represented by the formula (I) with fluorine gas to produce a tetrafluoro compound represented by the formula (II), (B) converting the tetrafluoro derivative represented by the formula (II) to a compound represented by the formula (III), and (C) reacting the compound represented by the formula (III) with an amine compound represented by the formula NH2R9 to produce a tetrafluoro nitrogen-containing heterocyclic compound represented by the formula (IV) or salt thereof.