175278-47-4 Usage
Uses
Used in Organic Synthesis:
2-[4-(TERT-BUTYL)PHENOXY]-5-NITROBENZALDEHYDE is used as a key intermediate in organic synthesis for the production of a variety of chemical compounds due to its reactive nitro and phenoxy functionalities.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-[4-(TERT-BUTYL)PHENOXY]-5-NITROBENZALDEHYDE is utilized as a building block for the synthesis of biologically active compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Dye Manufacturing:
2-[4-(TERT-BUTYL)PHENOXY]-5-NITROBENZALDEHYDE is employed as a chemical precursor in the production of dyes, leveraging its structural features to create a range of colorants for various applications.
Used in the Production of Fine Chemicals:
2-[4-(TERT-BUTYL)PHENOXY]-5-NITROBENZALDEHYDE is also used as a starting material in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including agriculture, fragrances, and flavorings, due to its versatile chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 175278-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,7 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 175278-47:
(8*1)+(7*7)+(6*5)+(5*2)+(4*7)+(3*8)+(2*4)+(1*7)=164
164 % 10 = 4
So 175278-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H17NO4/c1-17(2,3)13-4-7-15(8-5-13)22-16-9-6-14(18(20)21)10-12(16)11-19/h4-11H,1-3H3
175278-47-4Relevant academic research and scientific papers
Nitroarylhydroxymethylphosphonic acids as inhibitors of CD45
Beers, Scott A.,Malloy, Elizabeth A.,Wu, Wei,Wachter, Michael P.,Gunnia, Uma,Cavender, Druie,Harris, Crafford,Davis, Janet,Brosius, Ruth,Pellegrino-Gensey, J. Lee,Siekierka, John
, p. 2203 - 2211 (2007/10/03)
A series of nitroarylhydroxymethylphosphonic acids was synthesized and evaluated as inhibitors of CD45. It was discovered that both the alpha hydroxy and nitro groups are essential for activity. Potency is enhanced by the addition of a large lipophilic group on the aryl ring adjacent to the phosphonic acid moiety. Kinetics studies have shown that these compounds are competitive inhibitors and thus bind at the active site of this enzyme.
Xn:Harmful;
