28226-20-2 Usage
Description
2-(2,5-Dimethoxyphenylamino)ethanol is a chemical compound that belongs to the class of phenethylamines. It is commonly used as an intermediate in organic synthesis and pharmaceutical research. It is known for its potential applications in the development of new drugs and medications. 2-(2,5-DIMETHOXYPHENYLAMINO)ETHANOL is also used for various laboratory and research purposes due to its unique chemical properties. It is important to handle 2-(2,5-Dimethoxyphenylamino)ethanol with care and follow proper safety precautions when working with it in a laboratory setting.
Uses
Used in Pharmaceutical Research:
2-(2,5-Dimethoxyphenylamino)ethanol is used as an intermediate in pharmaceutical research for the development of new drugs and medications. Its unique chemical properties make it a valuable compound for creating innovative pharmaceutical products.
Used in Organic Synthesis:
2-(2,5-Dimethoxyphenylamino)ethanol is used as an intermediate in organic synthesis, allowing for the creation of various chemical compounds and materials.
Used in Laboratory and Research:
2-(2,5-Dimethoxyphenylamino)ethanol is used for various laboratory and research purposes due to its unique chemical properties, enabling scientists to explore new avenues in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 28226-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,2 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28226-20:
(7*2)+(6*8)+(5*2)+(4*2)+(3*6)+(2*2)+(1*0)=102
102 % 10 = 2
So 28226-20-2 is a valid CAS Registry Number.
28226-20-2Relevant articles and documents
One-pot synthesis of unsymmetrical N-heterocyclic carbene ligands from N-(2-iodoethyl)arylamine salts
Bhanu Prasad,Gilbertson, Scott R.
supporting information; experimental part, p. 3710 - 3713 (2011/02/28)
Image Presented An approach that provides symmetrical, unsymmetrical, and asymmetric N-heterocyclic carbene (NHC) ligands is reported. Reaction of iodoethanol with aniline provides N-(2-iodoethyl)arylamine salts that are then converted to the corresponding iodide. Reaction with aliphatic or aromatic amines followed by triethyl orthoformate was used to provide 26 different NHC ligands.
