15793-48-3 Usage
Uses
Used in Pharmaceutical Industry:
5-Chloro-2-ethoxyaniline is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with specific therapeutic properties.
Used in Dye Industry:
5-chloro-2-ethoxyaniline is utilized in the production of dyes, where its chemical properties contribute to the color and stability of the dyes produced.
Used in Agrochemical Industry:
5-Chloro-2-ethoxyaniline is employed in the synthesis of agrochemicals, which are essential for crop protection and enhancement of agricultural productivity.
Used in Rubber Chemical Industry:
It serves as a key component in the production of rubber chemicals, which are vital for improving the performance and durability of rubber products.
Used in Organic Chemical Synthesis:
5-Chloro-2-ethoxyaniline is used as a building block in the synthesis of other organic chemicals, expanding its applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 15793-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15793-48:
(7*1)+(6*5)+(5*7)+(4*9)+(3*3)+(2*4)+(1*8)=133
133 % 10 = 3
So 15793-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClNO/c1-2-11-8-4-3-6(9)5-7(8)10/h3-5H,2,10H2,1H3
15793-48-3Relevant academic research and scientific papers
N4-Phenyl modifications of N2-(2-hydroxyl)ethyl-6-(pyrrolidin-1-yl)-1,3,5-triazine-2,4-d iamines enhance glucocerebrosidase inhibition by small molecules with potential as chemical chaperones for Gaucher disease
Huang, Wenwei,Zheng, Wei,Urban, Daniel J.,Inglese, James,Sidransky, Ellen,Austin, Christopher P.,Thomas, Craig J.
, p. 5783 - 5789 (2008/02/13)
A series of 1,3,5-triazine-2,4,6-triamines were prepared and analyzed as inhibitors of glucocerebrosidase. Synthesis, structure activity relationships and the selectivity of chosen analogues against related sugar hydrolases enzymes are described.
