2188159-10-4 Usage
Heterocyclic compound
Yes
It contains a dioxoisoindoline ring and a 3-oxocyclobutane-1-carboxylate group, making it a heterocyclic compound.
Dioxoisoindoline ring
Present
The compound features a dioxoisoindoline ring, which is a fused ring system containing two oxygen atoms.
3-Oxocyclobutane-1-carboxylate group
Present
The compound also contains a 3-oxocyclobutane-1-carboxylate group, which is a four-membered ring with a carbonyl group and a carboxylate group.
Applications
Organic synthesis and pharmaceutical research
It is commonly used as a building block for various organic molecules and pharmaceutical compounds.
Potential biological activities
Unknown
Further research is needed to fully understand its potential applications and biological activities.
Medicinal properties
Unknown
Its medicinal properties are not yet fully understood and require additional research.
Solubility
Not specified
The solubility of 1,3-dioxoisoindolin-2-yl 3-oxocyclobutane-1-carboxylate in different solvents is not provided in the material.
Stability
Not specified
Information about the stability of 1,3-dioxoisoindolin-2-yl 3-oxocyclobutane-1-carboxylate under various conditions is not provided in the material.
Reactivity
Not specified
The reactivity of 1,3-dioxoisoindolin-2-yl 3-oxocyclobutane-1-carboxylate with other chemicals or under different conditions is not mentioned in the material.
Check Digit Verification of cas no
The CAS Registry Mumber 2188159-10-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,1,8,8,1,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2188159-10:
(9*2)+(8*1)+(7*8)+(6*8)+(5*1)+(4*5)+(3*9)+(2*1)+(1*0)=184
184 % 10 = 4
So 2188159-10-4 is a valid CAS Registry Number.
2188159-10-4Relevant academic research and scientific papers
Lu, Xiao-Yu,Li, Jing-Song,Hong, Mei-Lan,Wang, Jin-Yu,Ma, Wen-Jing
, p. 6979 - 6984 (2018)
A novel NiH-catalyzed decarboxylative hydroalkylation of internal alkynes has been developed. Trisubstituted olefins were obtained in moderate to good yields with good regioselectivities. The reaction involves cis addition of NiH to the internal alkyne. The reaction shows good functional-group tolerance.
