1411983-40-8 Usage
Description
3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(dipentylaMino)cyclohexyl]aMino]-3-Cyclobutene-1,2-dione is a cyclobutene-1,2-dione derivative with a complex molecular structure. It features amino groups attached to aromatic and cyclohexyl moieties, along with trifluoromethyl and dipentylamino groups, contributing to its chemical diversity. 3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(dipentylaMino)cyclohexyl]aMino]-3-Cyclobutene-1,2-dione may hold potential in medicinal and pharmaceutical research due to its unique structure and possible biological activities.
Uses
Used in Medicinal Research:
3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(dipentylaMino)cyclohexyl]aMino]-3-Cyclobutene-1,2-dione is used as a compound in medicinal research for its potential biological activities and unique molecular structure.
Used in Pharmaceutical Research:
3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(dipentylaMino)cyclohexyl]aMino]-3-Cyclobutene-1,2-dione is used as a compound in pharmaceutical research to explore its potential applications in drug development.
Further studies and evaluations are required to fully understand the properties and potential uses of 3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(dipentylaMino)cyclohexyl]aMino]-3-Cyclobutene-1,2-dione in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1411983-40-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,1,9,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1411983-40:
(9*1)+(8*4)+(7*1)+(6*1)+(5*9)+(4*8)+(3*3)+(2*4)+(1*0)=148
148 % 10 = 8
So 1411983-40-8 is a valid CAS Registry Number.
1411983-40-8Relevant articles and documents
Squaramide catalyzed enantioselective iodolactonization of allenoic acids
Kristianslund, Renate,Aursnes, Marius,Tungen, J?rn Eivind,Hansen, Trond Vidar
supporting information, p. 5232 - 5236 (2016/11/13)
An asymmetric iodolactonization reaction of allenoic acids has been extensively studied. Eight different chiral squaramides were prepared in a straightforward manner and investigated as organocatalysts. The reaction protocol is operationally simple to exe
