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1,5-dichloro-6,6,7,7-tetrafluoro-3-phenyl-2,4-dioxa-3-bora-bicyclo[3.2.0]heptane is a complex organic compound with the molecular formula C13H8BCl2F4O2. It features a unique bicyclic structure, with a boron atom at the center, connected to a phenyl group and two oxygen atoms forming a dioxaborane ring. The compound also contains two chlorine atoms and four fluorine atoms, which contribute to its overall stability and reactivity. This chemical is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds and the functionalization of various organic molecules. Its unique structure and properties make it a valuable tool in the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.

2848-15-9

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2848-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2848-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2848-15:
(6*2)+(5*8)+(4*4)+(3*8)+(2*1)+(1*5)=99
99 % 10 = 9
So 2848-15-9 is a valid CAS Registry Number.

2848-15-9Upstream product

2848-15-9Downstream Products

2848-15-9Relevant academic research and scientific papers

Reactions of hexafluorocyclobutanone with metalloid compounds

Parshall

, p. 52 - 54 (1965)

Hexafluorocyclobutanone, a highly polarized ketone, reacts with boron halides to give esters of 1-halohexafluorocyclobutanol. Similarly, silanes add to the ketone to give hexafluorocyclobutoxy derivatives. Phosphines add in the opposite direction to give 1-hydroxyhexafluorocyclobutylphosphines.

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