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Phenol, 4-(2-fluorophenoxy)-, also known as 4-(2-fluorophenoxy)phenol or 2-fluorophenol, 4'-hydroxy-, is an organic compound with the chemical formula C12H9FO2. It is a derivative of phenol, where one of the hydrogen atoms on the phenol ring is replaced by a 2-fluorophenoxy group. Phenol, 4-(2-fluorophenoxy)- is characterized by its molecular weight of 206.2 g/mol and a melting point of 47-49°C. It is a colorless to pale yellow solid and is soluble in organic solvents. 4-(2-fluorophenoxy)phenol is used in various applications, including as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications and properties, it is important to understand its chemical structure, reactivity, and safety considerations.

328-21-2

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328-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328-21-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 328-21:
(5*3)+(4*2)+(3*8)+(2*2)+(1*1)=52
52 % 10 = 2
So 328-21-2 is a valid CAS Registry Number.

328-21-2Downstream Products

328-21-2Relevant academic research and scientific papers

Quinoline derivative as well as preparation method and application thereof (by machine translation)

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Paragraph 0261; 0263-0267, (2019/11/28)

The invention provides a quinoline derivative and a composition containing the same. The invention also provides a method for preparing the derivative and application of the derivative and the composition to kill pests. (by machine translation)

Phenoxyphenoxypropionates, intermediates thereof and methods of preparation

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, (2008/06/13)

A method for preparing substituted phenoxyphenols which are useful in the preparation of herbicidal (phenoxyphenoxy)propionates is disclosed. The process involves the oxidation of substituted phenoxyphenones to the corresponding phenoxyphenyl esters and their conversion to the desired phenoxyphenol. Novel intermediates for the process are similarly disclosed.

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