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2-amino-5-chloro-N-ethylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32212-30-9

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32212-30-9 Usage

Derivative of

Benzamide

Substituents

Amino Group: Attached at the 2-position on the benzene ring
Chlorine Atom: Attached at the 5-position on the benzene ring
Ethyl Group: Attached to the nitrogen atom

Applications

Pharmaceutical Industry: Used for synthesizing various drugs
Medicinal Properties: Exhibits antiproliferative and anticancer properties
Research and Development: Utilized for creating new chemical entities and pharmaceutical products

Significance

Plays a significant role in medicinal and chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 32212-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32212-30:
(7*3)+(6*2)+(5*2)+(4*1)+(3*2)+(2*3)+(1*0)=59
59 % 10 = 9
So 32212-30-9 is a valid CAS Registry Number.

32212-30-9Upstream product

32212-30-9Downstream Products

32212-30-9Relevant academic research and scientific papers

Extending the biocatalytic scope of regiocomplementary flavin-dependent halogenase enzymes

Shepherd, Sarah A.,Karthikeyan, Chinnan,Latham, Jonathan,Struck, Anna-Winona,Thompson, Mark L.,Menon, Binuraj R. K.,Styles, Matthew Q.,Levy, Colin,Leys, David,Micklefield, Jason

, p. 3454 - 3460 (2015/05/27)

Flavin-dependent halogenases are potentially valuable biocatalysts for the regioselective halogenation of aromatic compounds. These enzymes, utilising benign inorganic halides, offer potential advantages over traditional non-enzymatic halogenation chemistry that often lacks regiocontrol and requires deleterious reagents. Here we extend the biocatalytic repertoire of the tryptophan halogenases, demonstrating how these enzymes can halogenate a range of alternative aryl substrates. Using structure guided mutagenesis we also show that it is possible to alter the regioselectivity as well as increase the activity of the halogenases with non-native substrates including anthranilic acid; an important intermediate in the synthesis and biosynthesis of pharmaceuticals and other valuable products. This journal is

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