62898-86-6 Usage
Heterocyclic organic compound
It is an organic compound that contains a ring structure with at least one heteroatom, which is an atom other than carbon, such as nitrogen (N) or oxygen (O), in the ring.
Use as an intermediate
The compound is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds, meaning it is a reactant in the production of other chemicals and drugs.
Potential biological and pharmacological activities
The chemical has been studied for its possible effects on living organisms and its potential therapeutic uses, including its role as an intermediate in the production of various drugs.
Building block for new drug molecules
Researchers are interested in using this compound as a starting point for the development of new drugs, due to its unique structure and properties.
Applications in organic synthesis and chemical research
The compound may have broader applications in the field of organic chemistry, as a useful building block or reactant in the synthesis of other complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 62898-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,9 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62898-86:
(7*6)+(6*2)+(5*8)+(4*9)+(3*8)+(2*8)+(1*6)=176
176 % 10 = 6
So 62898-86-6 is a valid CAS Registry Number.
62898-86-6Relevant articles and documents
Indium-Catalyzed Amide Allylation of N-Carbonyl Imides: Formation of Azaspiro-γ-lactones via Ring Opening-Reclosure
Sengoku, Tetsuya,Murata, Yusuke,Aso, Yuwa,Kawakami, Ai,Inuzuka, Toshiyasu,Sakamoto, Masami,Takahashi, Masaki,Yoda, Hidemi
, p. 5846 - 5849 (2015)
A novel and facile synthesis of azaspiro-γ-lactones with a methylene-lactam framework from N-carbonyl imides is described. Mechanistic investigations provide evidence for a two-step reaction process involving ZnCl2-promoted addition of β-amido allylindium species followed by an unexpectedly molecular-sieves-mediated ring opening-reclosure concomitantly with the loss of an N-carbonyl unit.
