73185-66-7 Usage
Structure
Quinoxalinone derivative with a methylamino group attached to the third position of the quinoxalinone ring
Pharmacological properties
Potential uses in the field of medicine
Unique chemical structure
Makes it an interesting target for further research and development
Potential biological activity
May have applications in drug discovery and development, particularly in the areas of neuroscience and neuropharmacology
Treatment of various diseases and disorders
May make it a valuable compound for further exploration.
Check Digit Verification of cas no
The CAS Registry Mumber 73185-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,8 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73185-66:
(7*7)+(6*3)+(5*1)+(4*8)+(3*5)+(2*6)+(1*6)=137
137 % 10 = 7
So 73185-66-7 is a valid CAS Registry Number.
73185-66-7Relevant articles and documents
Novel one-pot synthesis of 1-alkyl-2-(aryloxy)methyl-1H-pyrrolo[2,3-b]quinoxalines via copper-free Sonogashira coupling reaction
Keivanloo, Ali,Fakharian, Mahsa,Nabid, Mohammad Reza,Amin, Amir Hossein
, p. 151 - 160 (2019/03/12)
Abstract: A novel, simple, and efficient protocol is described for the synthesis of 1-alkyl-2-(aryloxy)methyl-1H-pyrrolo[2,3-b]quinoxalines via the one-pot reaction of phenol or 2-naphthol derivatives, propargyl bromide, and N-alkyl-3-chloroquinoxaline-2-amines in the presence of palladium catalyst. This one-pot reaction is carried out in the absence of any copper salt at room temperature. The reaction product is dependent on the nature of the base used. The use of morpholine, as the base, affords the final cyclized product, and triethylamine only gives the coupling product. Graphical abstract: [Figure not available: see fulltext.].
