743430-91-3 Usage
Ethylamine derivative
A compound derived from ethylamine (C2H5NH2) by modifying its structure, in this case, by attaching a fluorine-substituted benzo[d][1,3]dioxole ring structure.
Fluorine-substituted benzo[d][1,3]dioxole ring structure
A benzo[d][1,3]dioxole ring (a 3-membered oxygen-containing ring fused to a benzene ring) with a fluorine atom as a substituent, which can influence the compound's pharmacological properties and reactivity.
Medicinal chemistry and drug development applications
The compound is commonly used in the field of medicinal chemistry and drug development due to its potential pharmacological properties.
Potential pharmacological properties
The compound exhibits properties that may be beneficial in the treatment or management of various medical conditions, making it a valuable candidate for further study.
Valuable candidate for new drug development
The unique structure and pharmacological activity of 2-(6-fluoro-benzo[1,3]dioxol-5-yl)-ethylamine make it a promising candidate for the development of new drugs for a range of medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 743430-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,3,4,3 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 743430-91:
(8*7)+(7*4)+(6*3)+(5*4)+(4*3)+(3*0)+(2*9)+(1*1)=153
153 % 10 = 3
So 743430-91-3 is a valid CAS Registry Number.
743430-91-3Relevant academic research and scientific papers
A new approach to isoindoloisoquinolinones. A simple synthesis of nuevamine
Moreau, Anne,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre,Lebrun, Stéphane
, p. 6169 - 6176 (2007/10/03)
A convenient and versatile short step synthesis of isoindoloisoquinolinones, illustrated by the total synthesis of the alkaloid nuevamine 1a, is described. The tetracyclic lactam compounds were obtained by a tactical combination of the Parham procedure for the elaboration of the isoindolinone template and an aryne-mediated cyclization giving rise to the nitrogen containing six-membered heteroring unit.
