60290-06-4 Usage
Heterocyclic compound
Contains a benzene ring and a pyrrolopyridine ring This refers to the structure of the compound, which includes two different heterocyclic rings, providing a diverse range of chemical properties.
Chlorinated derivative
1-benzyl-7-chloro-1H-pyrrolo[2,3-c]pyridine is derived from 1-benzyl-1H-pyrrolo[2,3-c]pyridine with an added chlorine atom This highlights the modification of the original compound, resulting in a new compound with different properties and reactivity.
Pharmaceutical research
Commonly used as a potential building block for the synthesis of biologically active compounds This indicates the compound's role in creating new drugs and its importance in the pharmaceutical industry.
Reactivity and pharmacological properties
Influenced by the presence of benzyl and chloro substituents These functional groups in the molecule contribute to its unique reactivity and potential therapeutic effects.
Important intermediate
In the development of new drugs for various therapeutic applications This emphasizes the compound's significance in drug synthesis and its potential use in treating a wide range of medical conditions.
Unique structure
Attractive target for chemical synthesis and medicinal chemistry studies The compound's distinct structure makes it an interesting subject for further research and development in the field of chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 60290-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,9 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60290-06:
(7*6)+(6*0)+(5*2)+(4*9)+(3*0)+(2*0)+(1*6)=94
94 % 10 = 4
So 60290-06-4 is a valid CAS Registry Number.
60290-06-4Relevant articles and documents
Microwave-assisted acid-catalyzed nucleophilic heteroaromatic substitution: The synthesis of 7-amino-6-azaindoles
Nechayev, Maxim A.,Gorobets, Nikolay Yu.,Shishkina, Svetlana V.,Shishkin, Oleg V.,Kovalenko, Sergiy M.
, p. 1311 - 1321 (2015)
Derivatives of 7-amino-6-azaindole containing variable substituent in the amino group were synthesized via acid-catalyzed nucleophilic heteroaromatic substitution (SNHetarH+) using 7-chloro-6-azaindoles as substrates and aliphatic an
