1046468-30-7 Usage
Class of compounds
Pyrazolopyridine derivatives 1H-Pyrazolo[3,4-b]pyridin-3-amine, N-phenyl- belongs to a group of chemical compounds that have a pyrazolo[3,4-b]pyridine core structure.
Core structure
Pyrazolo[3,4-b]pyridine The core structure of 1H-Pyrazolo[3,4-b]pyridin-3-amine, N-phenyl- is a fusion of a pyrazole and a pyridine ring, with the pyrazole ring being attached to the third and fourth positions of the pyridine ring.
Amine group attachment
3rd position An amine group (-NH2) is attached to the third position of the pyrazolo[3,4-b]pyridine core, which can participate in various chemical reactions and interactions.
N-phenyl substitution
Phenyl group attached to amine nitrogen A phenyl group (a flat, six-carbon ring structure) is attached to the nitrogen atom of the amine group, which can influence the compound's properties and reactivity.
Potential applications
Medicinal chemistry and drug development 1H-Pyrazolo[3,4-b]pyridin-3-amine, N-phenyl- may exhibit biological activity and could be used as a building block for the synthesis of novel pharmaceutical compounds.
Other potential uses
Agrochemicals and materials science 1H-Pyrazolo[3,4-b]pyridin-3-amine, N-phenylmay also have applications in industries such as agrochemicals (e.g., pesticides, herbicides) and materials science (e.g., synthesis of new materials with specific properties).
Check Digit Verification of cas no
The CAS Registry Mumber 1046468-30-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,4,6 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1046468-30:
(9*1)+(8*0)+(7*4)+(6*6)+(5*4)+(4*6)+(3*8)+(2*3)+(1*0)=147
147 % 10 = 7
So 1046468-30-7 is a valid CAS Registry Number.
1046468-30-7Relevant academic research and scientific papers
An efficient route to 3-aminoindazoles and 3-amino-7-azaindazoles
Burke, Michael J.,Trantow, Brian M.
, p. 4579 - 4581 (2008/09/21)
A non-acidic procedure for the preparation of 3-aminoindazoles and 3-amino-7-azaindazoles from 2-fluoroaryl carboxylic acids is reported. The synthesis starts from readily available starting materials and uses mild and practical reaction conditions in a three-step overall procedure. Products were isolated for a number of examples, but yields varied significantly depending on electronic nature of the substituents.
