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Isopropyl 2,2,3,3,4,4,4-heptafluorobutyrate, also known as 2,2,3,3,4,4,4-heptafluoro-1-methylbutyl acetate, is a synthetic chemical compound with the molecular formula C7H9F7O2. It is a colorless liquid with a molecular weight of 264.14 g/mol. isopropyl 2,2,3,3,4,4,4-heptafluorobutyrate is characterized by its unique structure, which includes a heptafluorobutyrate group attached to an isopropyl group. It is primarily used as a solvent, particularly in the electronics industry for cleaning and etching processes, due to its low surface tension, high dielectric constant, and excellent solvency properties. Additionally, it has applications in the production of pharmaceuticals and agrochemicals. The compound is known for its low toxicity and environmental persistence, which makes it a preferred choice in certain industrial applications over more hazardous solvents.

425-23-0

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425-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 425-23-0 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, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 425-23:
(5*4)+(4*2)+(3*5)+(2*2)+(1*3)=50
50 % 10 = 0
So 425-23-0 is a valid CAS Registry Number.

425-23-0Relevant academic research and scientific papers

Homogeneous oxidation of alkanes: Role of rhodium–alkyl complexes

Chepaikin,Bezruchenko,Menchikova,Gekhman

, p. 389 - 392 (2017)

Catalytic systems RhCl3–KI–NaCl and RhCl3–Cu(OAcf)2–NaCl in aqueous perfluorinated carboxylic acids (CF3COOH, C3F7COOH) are effective in coupled oxidation of alkanes and carbon monoxide with dioxygen. In their presence, predominant is the outer-sphere oxidation of alkanes into respective esters (alcohols) with involvement of peroxo rhodium species as an oxidant (mechanism A). The process occurs partially by the inner-sphere mechanism B involving Rh–alkyl intermediates. Mechanism B is supported by (a) formation of alkyl chlorides, (b) synthesis of acetic acid in conversion of methane, and (c) positional selectivity in oxidation of propane.

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