1135292-74-8 Usage
Description
[1-(2-Ethoxyphenyl)ethyl]amine hydrochloride, with the molecular formula C10H16ClNO, is an organic compound derived from ethylamine and 2-ethoxyphenyl. It is a hydrochloride salt that is stable and easy to handle, making it suitable for use in laboratory settings. [1-(2-Ethoxyphenyl)ethyl]amine hydrochloride is known for its ability to interact with various biological targets, which makes it a promising candidate for further research in the field of medicinal chemistry.
Uses
Used in Pharmaceutical Research:
[1-(2-Ethoxyphenyl)ethyl]amine hydrochloride is used as a building block for the synthesis of various bioactive molecules. Its versatility in interacting with different biological targets allows for the development of new drugs with potential applications in treating a range of medical conditions.
Used in the Treatment of Medical Conditions:
In the field of medicine, [1-(2-Ethoxyphenyl)ethyl]amine hydrochloride has been studied for its potential applications in the treatment of various neurological disorders and psychiatric diseases. Its ability to interact with biological targets makes it a valuable compound for further research and development in these areas.
Used in Medicinal Chemistry:
As a promising candidate for medicinal chemistry, [1-(2-Ethoxyphenyl)ethyl]amine hydrochloride is utilized in the development of new drugs and therapies. Its stability and ease of handling in laboratory settings contribute to its potential for use in creating novel pharmaceutical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1135292-74-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,5,2,9 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1135292-74:
(9*1)+(8*1)+(7*3)+(6*5)+(5*2)+(4*9)+(3*2)+(2*7)+(1*4)=138
138 % 10 = 8
So 1135292-74-8 is a valid CAS Registry Number.
1135292-74-8Relevant articles and documents
Comparison of different reducing systems in the synthesis of functionally substituted benzylamines from alkyl aryl ketones and aromatic aldehydes
Musatov,Starodubtseva,Turova,Kurilov,Vinogradov,Rakishev,Struchkova
experimental part, p. 1021 - 1028 (2010/11/03)
Different synthetic approaches to functionally substituted benzylamines were examined: reductive amination of alkyl aryl ketones and reduction of aromatic aldehyde oximes. The most efficient procedures were used to prepare a series of previously unknown h
