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Isopropyl (fluoro)phenylphosphinate is a chemical compound with the molecular formula C9H10FO2P. It is an organophosphorus compound, which is characterized by the presence of a phosphorus atom bonded to carbon and other elements. This specific compound features an isopropyl group (a three-carbon branched alkyl group) and a fluorophenyl group (a phenyl ring with a fluorine atom attached). Isopropyl (fluoro)phenylphosphinate is known for its potential applications in the synthesis of various phosphorus-containing compounds and as a reagent in organic chemistry. Due to its unique structure, it may also have implications in the development of new materials or pharmaceuticals, although specific uses would depend on further research and development.

2145-64-4

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2145-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2145-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,4 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2145-64:
(6*2)+(5*1)+(4*4)+(3*5)+(2*6)+(1*4)=64
64 % 10 = 4
So 2145-64-4 is a valid CAS Registry Number.

2145-64-4Downstream Products

2145-64-4Relevant academic research and scientific papers

Copper-promoted oxidative-fluorination of arylphosphine under mild conditions

Liu, Na,Mao, Liu-Liang,Yang, Bin,Yang, Shang-Dong

, p. 10879 - 10882 (2014)

An efficient method for the synthesis of phosphoric fluoride via oxidative coupling between hydrophosphine oxide and NaF is reported. DDQ serves as the oxidizing reagent as well as the hydrogen acceptor. The process involves a Cu(ii) catalysis and exhibits great functional group tolerance under mild reaction conditions. the Partner Organisations 2014.

Anomalous reaction of ethyl bromofluoro- and difluoro-acetates with dialkylphosphonites

Durst,Rohrbaugh,Smith,Nilles,Connell,Laramee,Munavalli

experimental part, p. 2655 - 2668 (2009/09/25)

The Michaelis-Arbuzov reaction of ethyl α-bromo-α-fluoro- and α, α-difluoro-acetates with dialkyl phenylphosphonites leads to the formation of unusual products including a fluorophosphinate. The reaction of ethyl bromofluoracetate with diisopropyl- and dimethyl-phenylphosphonites furnishes a complex mixture of eight and five compounds respectively. Five different compounds are obtained when ethyl bromodifluoroacetate is reacted with diisopropyl phenylphosphonite. Dimethyl phenylphosphonite yields three compounds when heated with bromochloromethane. The probable mechanism of formation of the compounds and their mass spectral characterization using GC-MS, tandem MS-MS and DART techniques are presented in this paper. Copyright Taylor & Francis Group, LLC.

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