80493-71-6 Usage
Molecular structure
Contains an imidazo[1,2-a]pyridin-3-ylamine core attached to a 4-methoxyphenyl group.
Type of compound
Heterocyclic amine.
Usage
Employed in pharmaceutical research and drug development.
Potential properties
May exhibit biological activity or therapeutic applications due to its unique molecular structure.
Imidazo[1,2-a]pyridine core
Indicates possible specific interactions with biological targets, making it a topic of interest for medicinal chemistry.
4-Methoxyphenyl group
Contributes to the compound's physicochemical properties and potential biological effects.
Further research
Additional studies and testing may be required to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 80493-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80493-71:
(7*8)+(6*0)+(5*4)+(4*9)+(3*3)+(2*7)+(1*1)=136
136 % 10 = 6
So 80493-71-6 is a valid CAS Registry Number.
80493-71-6Relevant articles and documents
Skeletal diverse synthesis of N-fused polycyclic heterocycles via the sequence of Ugi-type MCR and CuI-catalyzed coupling/tandem Pictet-Spengler reaction
Tyagi, Vikas,Khan, Shahnawaz,Bajpai, Vikas,Gauniyal, Harsh M.,Kumar, Brijesh,Chauhan, Prem M. S.
experimental part, p. 1414 - 1421 (2012/03/11)
Several diversity-oriented syntheses of N-fused polycyclic heterocycles have been demonstrated but most of them are based on point diversity within the same library and usually involve time-consuming sequential multistep syntheses, which also suffer from
Cyclisation Reactions of some 3-Nitrosoimidazo-pyridines and -pyrimidines. Ring-opening/Ring-closure Reactions with Triethyl Phosphite: Reassignment by X-Ray Crystal Structure and Nuclear Magnetic Resonance
Teulade, Jean C.,Escale, Roger,Viols, Henry,Chapat, Jean P.,Grassy, Gerard,et al.
, p. 2663 - 2667 (2007/10/02)
Deoxygenation of 3-nitroso-2-phenylimidazo-pyridines and -pyrimidines with triethyl phosphite does not lead to the products described in the literature as pyrido- and pyrimido-imidazoindoles (3) and (4), but to the open-chain derivatives, N-(2-pyri
