120422-92-6 Usage
Core Structure
Heterocyclic organic compound with a pyrazolo-pyridinone core structure
Application
Commonly used in pharmaceutical research and development of potential therapeutic agents
Biological Activities
Known for its potential pharmacological properties, making it of interest for medical and pharmaceutical research
Importance
Considered an important compound for researchers in the medical and pharmaceutical fields, indicating its significance in drug discovery and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 120422-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120422-92:
(8*1)+(7*2)+(6*0)+(5*4)+(4*2)+(3*2)+(2*9)+(1*2)=76
76 % 10 = 6
So 120422-92-6 is a valid CAS Registry Number.
120422-92-6Relevant articles and documents
A General Procedure for the Synthesis of Pyrido-Condensed Heterocycles
Donati, Donato,Ferrini, Serena,Fusi, Stefania,Ponticelli, Fabio
, p. 2518 - 2524 (2003)
Reaction of 4-substituted isoxazolo[4,5-c]- and [5,4-b]pyridines with Mo(CO)6 in refluxing methanol is an efficient and versatile procedure for the preparation of functionalized pyrido-condensed heterocycles containing from five to eight atoms in the ring.
Photochemical rearrangements of 3-methyliscxazolopyridines
Donati, Donato,Fusi, Stefania,Ponticelli, Fabio,Tedeschi, Piero
, p. 1899 - 1905 (2007/10/02)
Irradiation in water-saturated ethyl ether of isoxazolopyridines 1a,e, beside the corresponding oxazolopyridines 2a,e, leads to N-methylcarboxamides 3a,e via 1-2 shift of the methyl group. The isoxazolopyridine 5, bearing a hydrazino group in 4-position, rearranges only to l-aminopyrazolopyridine 6.
