503417-39-8 Usage
Uses
Used in Organic Synthesis:
1-(NAPHTHALEN-1-YL)CYCLOPROPANAMINE is used as a key intermediate in organic synthesis for the creation of complex organic molecules. Its unique structure allows for a variety of chemical reactions, facilitating the synthesis of diverse compounds with potential applications across different industries.
Used in Drug Discovery:
In the pharmaceutical sector, 1-(NAPHTHALEN-1-YL)CYCLOPROPANAMINE is utilized as a starting material for the development of new drugs. Its structural attributes make it a valuable component in the design and synthesis of innovative therapeutic agents.
Used in Pharmaceutical Production:
1-(NAPHTHALEN-1-YL)CYCLOPROPANAMINE is employed as a fundamental building block in the production of various pharmaceuticals. Its incorporation into drug molecules can enhance their efficacy, selectivity, and pharmacokinetic properties.
Used in Agrochemicals:
1-(NAPHTHALEN-1-YL)CYCLOPROPANAMINE also finds application in the agrochemical industry, where it is used as a starting material for the synthesis of agrochemicals, contributing to the development of effective crop protection agents.
Used in Medicinal Chemistry Research:
1-(NAPHTHALEN-1-YL)CYCLOPROPANAMINE is used as a subject of research in medicinal chemistry due to its potential anti-inflammatory and anti-cancer properties. Its exploration in this field aims to uncover new therapeutic avenues for the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 503417-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,4,1 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 503417-39:
(8*5)+(7*0)+(6*3)+(5*4)+(4*1)+(3*7)+(2*3)+(1*9)=118
118 % 10 = 8
So 503417-39-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H13N/c14-13(8-9-13)12-7-3-5-10-4-1-2-6-11(10)12/h1-7H,8-9,14H2
503417-39-8Relevant articles and documents
A direct synthesis of 1-aryl- and 1-alkenylcyclopropylamines from aryl and alkenyl nitriles
Bertus, Philippe,Szymoniak, Jan
, p. 7133 - 7136 (2007/10/03)
The reaction of various aromatic nitriles with 1.1 equiv of Ti(Oi-Pr)4 and 2.2 equiv of EtMgBr followed by addition of a Lewis acid gave 1-aryl cyclopropylamines in 43-76% yields. Under similar conditions, conjugated alkene-nitriles afford 1-alkenylcyclopropylamines (42-65%).
