56370-30-0 Usage
Description
4-ETHOXYPHENETHYLAMINE, also known as 2-(4-Ethoxyphenyl)ethanamine Hydrochloride, is an organic compound with a molecular structure that features an ethoxyphenyl group attached to an ethanamine backbone. It is a derivative of phenylethylamine, which is a class of compounds known for their diverse range of pharmacological properties and potential applications in the medical and pharmaceutical industries.
Uses
Used in Pharmaceutical Research:
4-ETHOXYPHENETHYLAMINE is used as a research compound for studying the pharmacological properties of phenylethylamine derivatives. Its unique structure allows scientists to explore its potential interactions with various biological targets, which could lead to the development of new drugs with specific therapeutic effects.
Used in Drug Development:
In the pharmaceutical industry, 4-ETHOXYPHENETHYLAMINE serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its versatile chemical structure enables the creation of novel drug candidates with potential applications in treating a wide range of medical conditions.
Used in Neuropharmacology:
4-ETHOXYPHENETHYLAMINE is also utilized in neuropharmacological research, where it helps researchers understand the mechanisms of action of phenylethylamine-based compounds on the central nervous system. This knowledge can be applied to develop new treatments for neurological and psychiatric disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 56370-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,7 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56370-30:
(7*5)+(6*6)+(5*3)+(4*7)+(3*0)+(2*3)+(1*0)=120
120 % 10 = 0
So 56370-30-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO/c1-2-12-10-5-3-9(4-6-10)7-8-11/h3-6H,2,7-8,11H2,1H3
56370-30-0Relevant articles and documents
Syntheses of a selective peroxisome proliferator activated receptor modulator and practical new preparations of 2-(4-Alkoxyphenyl) ethylamines t
Magnus, Nicholas A.,Astleford, Bret A.,Brennan, John,Stout, James R.,Tharp-Taylor, Roger W.
experimental part, p. 280 - 284 (2010/04/22)
This article describes chemistry that was developed to give access to multigram quantities of the selective peroxisome proliferator activated receptor modulator (SPPARM), compound 1.1 Fischer esteriflcations, phase transfer-catalyzed alkylations, amide couplings, crystallizations, and a new synthesis were developed to accomplish this task. In addition, an efficient method for preparing 2-(4-alkoxyphenyl) ethylamines 7a - d from tyramine 9 was developed that involves O-alkylation of intermediate Schiff base 11 and subsequent acid-catalyzed hydrolysis to afford the target molecules as crystalline hydrochloride salts.
