1201633-52-4 Usage
Uses
Used in Organic Synthesis:
[1-(4-Ethoxyphenyl)propyl]amine hydrochloride is used as a precursor or reagent in organic synthesis for its ability to facilitate the formation of various complex organic molecules. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [1-(4-Ethoxyphenyl)propyl]amine hydrochloride is used as a key intermediate in the development of new drugs. Its structural features can be exploited to create novel compounds with potential therapeutic applications, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
[1-(4-Ethoxyphenyl)propyl]amine hydrochloride is also utilized in chemical research to study the properties and reactions of amine and ether functional groups. It can provide insights into the reactivity and selectivity of these groups, aiding in the understanding of fundamental chemical processes and the design of new synthetic routes.
Used in Material Science:
[1-(4-Ethoxyphenyl)propyl]amine hydrochloride may find applications in material science, where it could be used to develop new polymers or other materials with specific properties. Its ability to form complexes or participate in condensation reactions could be harnessed to create materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1201633-52-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,3 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1201633-52:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*3)+(3*3)+(2*5)+(1*2)=94
94 % 10 = 4
So 1201633-52-4 is a valid CAS Registry Number.
1201633-52-4Relevant academic research and scientific papers
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
