1024024-65-4 Usage
Uses
Used in Fire Suppression:
FE-36 is used as a fire extinguishing agent for its effectiveness in putting out fires involving flammable liquids, electrical equipment, and combustible materials. Its high heat absorption capacity and low toxicity make it a suitable choice for environments with sensitive electronic equipment and other materials that could be damaged by traditional firefighting agents.
Used as a Replacement for Halon-based Extinguishing Agents:
Given its low global warming potential, FE-36 serves as an environmentally friendly alternative to halon-based extinguishing agents. This makes it a preferred choice for applications where reducing the environmental impact of fire suppression is a priority.
Used in Sensitive Electronic Equipment Protection:
Due to its low toxicity and high stability, FE-36 is particularly useful in protecting sensitive electronic equipment from damage during fire incidents. It ensures that the firefighting process does not cause additional harm to the equipment, thus preserving its functionality and value.
Used in Various Industries:
FE-36 is utilized across different industries where fire safety is a concern, including but not limited to aviation, automotive, manufacturing, and data centers. Its versatility and effectiveness make it a valuable asset in these sectors for preventing and managing fires.
Check Digit Verification of cas no
The CAS Registry Mumber 1024024-65-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,4,0,2 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1024024-65:
(9*1)+(8*0)+(7*2)+(6*4)+(5*0)+(4*2)+(3*4)+(2*6)+(1*5)=84
84 % 10 = 4
So 1024024-65-4 is a valid CAS Registry Number.
1024024-65-4Relevant academic research and scientific papers
Bazhin,Gorbunova,Zapevalov,Kirichenko,Saloutin
, p. 656 - 659 (2007)
The reaction of fluorine-containing glycidyl ethers with various alcohols (i-PrOH, MeOH, PhOH, 2,2,3,3-tetrafluoropropanol) in basic medium resulted in products of regioselective opening of the oxirane ring. In reaction of 2,2,3,3-tetrafluoropropyloxymeth
Non-perfluorinated short carbon chain intermediate Monomer and synthesis method thereof
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Paragraph 0067-0075, (2021/08/25)
The invention discloses a non-perfluorocarbon chain intermediate, a monomer and a synthesis method thereof. The structural formula of the non-perfluorinated short carbon chain intermediate is as follows. In the formula (n ≤ 6), the structural formula of the non-perfluorinated short carbon chain monomer is shown in the specification. Therein, n rounds of R CH2 are selected from the group consisting of: (xCH)-(R). 3 ]: xThe non-perfluorinated short carbon chain intermediate comprises two or more than two non-perfluorinated short carbon chains, has a good rejection function and is not easy to break, has low instant toxicity, biodegradability, no environmental pollution and biological accumulation, does not damage the environment, influences human health risks, and has a wide application prospect.
