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1,2,3,3,4,5,5-heptafluorocyclopentene is a halogenated cycloalkene with the molecular formula C5F7H. It is a colorless liquid with a strong, pungent odor. 1,2,3,3,4,5,5-heptafluorocyclopentene is characterized by the presence of seven fluorine atoms and one hydrogen atom attached to a five-membered cyclopentene ring. Due to its highly fluorinated structure, 1,2,3,3,4,5,5-heptafluorocyclopentene exhibits unique chemical and physical properties, such as high thermal stability, low reactivity, and a low boiling point. These properties make it a valuable intermediate in the synthesis of various fluorinated compounds, including pharmaceuticals, agrochemicals, and specialty materials. Additionally, its low reactivity and high stability make it a potential candidate for use in industrial applications, such as refrigerants and fire-suppressing agents.

2344-15-2

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2344-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2344-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2344-15:
(6*2)+(5*3)+(4*4)+(3*4)+(2*1)+(1*5)=62
62 % 10 = 2
So 2344-15-2 is a valid CAS Registry Number.

2344-15-2Relevant academic research and scientific papers

Method for preparing halogenated pentacyclic olefin by gas-phase isomerization reaction

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Paragraph 0037; 0078; 0079, (2017/12/30)

The invention relates to a method for preparing halogenated pentacyclic olefin by gas-phase isomerization reaction. The method comprises the following steps of: by adopting the halogenated pentacyclic olefin C5HxFyClz as a material, under the existence of an isomerization catalyst, generating the gas-phase isomerization reaction to obtain isomers of the halogenated pentacyclic olefin, wherein X is an integer from 0 to 2, Y is an integer from 4 to 7, Z is an integer from 0 to 4, the sum of X and Y and Z is 8, and the isomerization catalyst is prepared by adopting at least one of lithium fluoride, potassium fluoride, sodium fluoride, rubidium fluoride or cesium fluoride as an active component and loading the active component on at least one of carriers such as aluminium fluoride, magnesium fluoride, iron fluoride, chromium fluoride and zinc fluoride. The method has the advantages that the material is easy to obtain, the isomerization catalyst is low in price, the yield of the isomer is higher, and the method is applicable to large-scale preparation of the isomers of the halogenated pentacyclic olefin by gas-phase reaction.

Activation of aromatic, aliphatic, and olefinic carbon-fluorine bonds using Cp*2HfH2

Rieth, Ryan D.,Brennessel, William W.,Jones, William D.

, p. 2839 - 2847 (2008/02/10)

The hafnium hydride Cp*2HfH2 is reacted with a series of fluorocarbons to examine the scope of C-F bond activation. Aromatic, vinylic, and aliphatic C-F bonds all show some degree of reactivity, and possible mechanisms are discussed. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

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