103733-35-3 Usage
General Description
The chemical "<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 compound with a long and intricate name. It is a derivative of 1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid and ethyl ester, and it contains an ethoxycarbonyl group and a phenylpropylamino group. The compound has a chiral center and is in the (S)-configuration. It is a potential pharmacophore for drug development due to its structure and functional groups. <3S-<2>,3R*>-2-<2-<<1-(ethoxycarbonyl)-3-phenylpropyl>amino>-1-oxopropyl>-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, ethyl ester could potentially have pharmaceutical applications due to its complex structure and is likely to be used in research for various medical purposes.
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.
