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Phenyl-phosphonic acid monopentyl ester is an organic compound with the chemical formula C11H15O3P. It is a derivative of phenylphosphonic acid, where one of the hydrogen atoms is replaced by a pentyl group (a five-carbon alkyl chain). phenyl-phosphonic acid monopentyl ester is a colorless liquid with a density of 1.1 g/cm3 and a boiling point of 310°C. It is soluble in organic solvents and has a molecular weight of 222.21 g/mol. Phenyl-phosphonic acid monopentyl ester is used in various applications, including as a flame retardant, a plasticizer, and a stabilizer in the chemical industry. It is also known for its potential use as a pesticide and as an intermediate in the synthesis of other phosphorus-containing compounds. Due to its phosphorus content, it may have unique properties in these applications, such as enhancing thermal stability or providing resistance to degradation.

7670-97-5

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7670-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7670-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,7 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7670-97:
(6*7)+(5*6)+(4*7)+(3*0)+(2*9)+(1*7)=125
125 % 10 = 5
So 7670-97-5 is a valid CAS Registry Number.

7670-97-5Downstream Products

7670-97-5Relevant academic research and scientific papers

Microwave-assisted esterification of P-acids

ábrányi-Balogh, Péter,Harsági, Nikoletta,Keglevich, Gy?rgy,Kiss, Nóra Zsuzsa

, (2021/10/25)

The possibilities for the preparation of dialky phenylphosphonates were evaluated. On the one hand, the oxidation of phenyl-H-phosphinates gave the corresponding phenylphosphonic acid monoesters. On the other hand, phenylphosphonates may be prepared by MW-assisted direct esterification of phenylphosphonic acid. The reaction with alcohols was performed under MW irradiation in the presence of an ionic liquid as the catalyst. The second ester function was established by alkylating esterification carried out with alkyl halides in the presence of triethylamine under MW conditions.

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