47154-24-5 Usage
Heterocyclic structure
The compound has a ring structure containing both carbon and nitrogen atoms.
Pyrazolo[4,3-c]pyridine family
It belongs to a family of compounds with a specific arrangement of nitrogen atoms in the pyridine ring.
1,3-Diphenyl substitution
The compound has two phenyl groups attached to the 1 and 3 positions of the pyrazolo[4,3-c]pyridine nucleus.
Potential biological activities
It has been studied for its possible antimicrobial, anti-inflammatory, and antitumor properties.
Organic synthesis
The compound is used as a building block in the synthesis of various organic compounds due to its unique structural features.
Pharmaceutical and synthetic chemistry applications
The compound has potential uses in both the pharmaceutical industry and in synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 47154-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,1,5 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 47154-24:
(7*4)+(6*7)+(5*1)+(4*5)+(3*4)+(2*2)+(1*4)=115
115 % 10 = 5
So 47154-24-5 is a valid CAS Registry Number.
47154-24-5Relevant academic research and scientific papers
Synthesis of indazoles and azaindazoles by intramolecular aerobic oxidative C-N coupling under transition-metal-free conditions
Hu, Jiantao,Xu, Huacheng,Nie, Pengju,Xie, Xiaobo,Nie, Zongxiu,Rao, Yu
supporting information, p. 3932 - 3938 (2014/04/17)
A transition-metal-free oxidative C-N coupling method has been developed for the synthesis of 1H-azaindazoles and 1H-indazoles from easily accessible hydrazones. The procedure uses TEMPO, a basic additive, and dioxygen gas as the terminal oxidant. This reaction demonstrates better reactivity, functional group tolerance, and broader scope than comparable metal catalyzed reactions. A transition-metal-free oxidative C-N coupling method has been developed for the synthesis of 1H-azaindazoles and 1H-indazoles from easily accessible hydrazones (see scheme). The procedure uses TEMPO, a basic additive, and dioxygen gas as the terminal oxidant. This reaction demonstrates better reactivity, functional group tolerance, and broader scope than comparable metal catalyzed reactions. TEMPO=2,2,6,6-tetramethyl-1-piperidinyloxy.
