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(2-chloro-2-oxo-1-phenylethyl)ammonium chloride, also known as alpha-chloracetophenone ammonium chloride, is a quaternary ammonium compound with the molecular formula C8H10ClNO2. It is a white crystalline solid that is soluble in water and is commonly used as a reagent in organic chemistry for the synthesis of various compounds.

5321-31-3

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5321-31-3 Usage

Uses

Used in Organic Chemistry:
(2-chloro-2-oxo-1-phenylethyl)ammonium chloride is used as a reagent for the synthesis of various compounds, making it a valuable component in organic chemistry.
Used in Pharmaceutical Production:
(2-chloro-2-oxo-1-phenylethyl)ammonium chloride is used as an intermediate in the production of pharmaceuticals, contributing to the development of important medicinal products.
Used in Agrochemical Production:
(2-chloro-2-oxo-1-phenylethyl)ammonium chloride is also used in the production of agrochemicals, playing a role in the creation of essential products for agriculture.
Used in Other Industrial Applications:
(2-chloro-2-oxo-1-phenylethyl)ammonium chloride serves as an intermediate in a variety of industrial applications, highlighting its versatility and importance in different sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 5321-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5321-31:
(6*5)+(5*3)+(4*2)+(3*1)+(2*3)+(1*1)=63
63 % 10 = 3
So 5321-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO.ClH/c9-8(11)7(10)6-4-2-1-3-5-6;/h1-5,7H,10H2;1H

5321-31-3Relevant academic research and scientific papers

Application of Yeast-Catalyzed Reductions to Synthesis of (2R,3S)-Phenylisoserine

Kearns, Jeff,Kayser, Margaret

, p. 2845 - 2848 (1994)

A simple synthesis of (2R,3S)-phenylisoserine, a precursor of the C-13 side chain of Taxol (paclitaxel), utilising yeast-catalyzed reduction to generate a second chiral centre is reported.This short enantioselective series of transformations can be readily adapted to large scale production of a variety of N-substituted paclitaxel analogues.

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