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2-(3-fluoro-4-hydroxyphenyl)ethylammonium chloride is a chemical compound with the molecular formula C8H10ClFNO. It is an organic salt derived from the combination of 3-fluoro-4-hydroxyphenylethylamine and hydrochloric acid. 2-(3-fluoro-4-hydroxyphenyl)ethylammonium chloride features a fluorinated phenyl ring, which imparts unique electronic properties due to the presence of the fluorine atom. The hydroxyl group provides a site for potential hydrogen bonding, while the ammonium group confers a positive charge, making the compound a zwitterion. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds. The compound's properties, such as its reactivity and solubility, can be influenced by the presence of the fluorine atom and the charged ammonium group, making it a potentially valuable building block in the development of new drugs and materials.

458-33-3

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458-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 458-33-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 458-33:
(5*4)+(4*5)+(3*8)+(2*3)+(1*3)=73
73 % 10 = 3
So 458-33-3 is a valid CAS Registry Number.

458-33-3Upstream product

458-33-3Downstream Products

458-33-3Relevant academic research and scientific papers

Nucleophilic deoxyfluorination of catechols

Nemoto, Hiroyuki,Nishiyama, Tsuyoshi,Akai, Shuji

supporting information; experimental part, p. 2714 - 2717 (2011/06/28)

Nucleophilic deoxyfluorinaiton of one of the two hydroxyl groups of catechols has been developed via the Umpolung concept. This method was successively applied to naturally occurring catechols, such as catechins and dopamine, to produce novel fluorinated

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