103733-35-3 Usage
Description
<3S-<2>,3R>-2-<2-<<1-(ethoxycarbonyl)-3-phenylpropyl>amino>-1-oxopropyl>-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, ethyl ester is a complex organic compound derived from 1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid and ethyl ester. It features an ethoxycarbonyl group and a phenylpropylamino group, with a chiral center in the (S)-configuration. <3S-<2>,3R>-2-<2-<<1-(ethoxycarbonyl)-3-phenylpropyl>amino>-1-oxopropyl>-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, ethyl ester is a potential pharmacophore for drug development due to its intricate structure and functional groups.
Uses
Used in Pharmaceutical Applications:
<3S-<2>,3R>-2-<2-<<1-(ethoxycarbonyl)-3-phenylpropyl>amino>-1-oxopropyl>-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, ethyl ester is used as a potential pharmacophore for drug development due to its complex structure and functional groups, which may offer various therapeutic benefits.
Used in Research and Development:
In the field of medicinal chemistry, <3S-<2>,3R>-2-<2-<<1-(ethoxycarbonyl)-3-phenylpropyl>amino>-1-oxopropyl>-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, ethyl ester is used as a compound for research and development. Its unique structure and functional groups make it a valuable candidate for exploring new therapeutic agents and understanding its interactions with biological targets.
Used in Drug Design and Optimization:
<3S-<2>,3R>-2-<2-<<1-(ethoxycarbonyl)-3-phenylpropyl>amino>-1-oxopropyl>-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, ethyl ester is used as a starting point for drug design and optimization. Its complex structure provides a foundation for modifying and improving its pharmacological properties, potentially leading to the development of novel therapeutic agents.
Used in Chemical Synthesis:
In the chemical synthesis industry, <3S-<2>,3R>-2-<2-<<1-(ethoxycarbonyl)-3-phenylpropyl>amino>-1-oxopropyl>-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, ethyl ester is used as a key intermediate or building block for the synthesis of more complex molecules with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 103733-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,3 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103733-35:
(8*1)+(7*0)+(6*3)+(5*7)+(4*3)+(3*3)+(2*3)+(1*5)=93
93 % 10 = 3
So 103733-35-3 is a valid CAS Registry Number.
103733-35-3Relevant articles and documents
The Baeyer-Villiger Oxidation of Aromatic Aldehydes and Ketones with Hydrogen Peroxide Catalyzed by Selenium Compounds
Syper, Ludwik
, p. 167 - 172 (2007/10/02)
A series of organoselenium compounds was investigated as activators of hydrogen peroxide in the Baeyer-Villiger oxidation.As a result, a convenient and cheap method for transformation of aromatic aldehydes, having polycondensed ring systems or electron-donating substituents, and polymethoxy derivatives of acetophenone, into phenols was elaborated.This method utilizes hydrogen peroxide activated by areneseleninic acids, as oxidizing agent.
