61702-02-1 Usage
Uses
Used in Pharmaceutical Industry:
(1Z)-N-(5-methylpyridin-2-yl)-1-[(5-methylpyridin-2-yl)imino]-1H-isoindol-3-amine is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique molecular structure may allow it to interact with biological targets in novel ways, offering the possibility of treating various diseases and conditions.
Used in Chemical Research:
In the field of chemical research, (1Z)-N-(5-methylpyridin-2-yl)-1-[(5-methylpyridin-2-yl)imino]-1H-isoindol-3-amine serves as a subject for studying the properties and reactions of heterocyclic compounds. Its complex structure provides opportunities for investigating new synthetic pathways and understanding its reactivity, which could lead to the discovery of related compounds with useful properties.
Used in Material Science:
(1Z)-N-(5-methylpyridin-2-yl)-1-[(5-methylpyridin-2-yl)imino]-1H-isoindol-3-amine may be utilized in material science for the development of new materials with specific properties. Its heterocyclic nature could contribute to the creation of materials with unique electronic, optical, or mechanical characteristics, depending on its interaction with other molecules or elements.
Check Digit Verification of cas no
The CAS Registry Mumber 61702-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61702-02:
(7*6)+(6*1)+(5*7)+(4*0)+(3*2)+(2*0)+(1*2)=91
91 % 10 = 1
So 61702-02-1 is a valid CAS Registry Number.
61702-02-1Relevant articles and documents
Metal free direct formation of various substituted pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5-amines and their further functionalization
Tber,Hiebel,Allouchi,El Hakmaoui,Akssira,Guillaumet,Berteina-Raboin
, p. 35201 - 35210 (2015)
Original substituted pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5-amines have been prepared following a Groebke-Blackburn-Bienaymé MCR combined with an N-deprotection and a spontaneous final cyclization step in moderate to good yields. The flexibility of the described method enables the introduction of diverse groups in the 6 and 7 positions on the resulting scaffold using commercially available starting materials. Furthermore, a Buchwald-Hartwig cross coupling with a wide range of aryl and hetaryl halides has been successfully reported using our heterocyclic primary amine derivatives.
