1350980-14-1 Usage
Functional Group
Thiourea
Explanation
A carbon atom double bonded to a sulfur atom and single bonded to two amino groups.
Explanation
A bicyclic amine with a quinoline ring system attached to the thiourea group.
Explanation
The presence of a chiral center with an (R)-configuration.
Explanation
A phenyl group substituted with two trifluoromethyl groups and a 5-ethyl group on the quinuclidine moiety.
Explanation
Due to its unique structure and properties, this compound may have applications in the development of new drugs and therapies.
Explanation
The molecular formula represents the total number of each type of atom present in the compound.
Explanation
The molecular weight is the sum of the atomic weights of all the atoms in the molecule.
Explanation
The compound's solubility is not provided, but based on its structure, it is likely to be soluble in organic solvents like DMSO or methanol.
Explanation
The stability of the compound is not provided, but the presence of a thiourea group and multiple fluorine atoms suggests it may be sensitive to hydrolysis and oxidation under certain conditions.
Structural Elements
Quinuclidine moiety and quinoline ring system
Stereochemistry
(R)-configuration at the chiral center
Substituents
3,5-bis(trifluoromethyl)phenyl and 5-ethyl group
Potential Applications
Medicinal and pharmaceutical research
Molecular Weight
Approximately 542.57 g/mol
Solubility
Unknown, but likely soluble in organic solvents
Stability
Unknown, but may be sensitive to hydrolysis and oxidation
Check Digit Verification of cas no
The CAS Registry Mumber 1350980-14-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,9,8 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1350980-14:
(9*1)+(8*3)+(7*5)+(6*0)+(5*9)+(4*8)+(3*0)+(2*1)+(1*4)=151
151 % 10 = 1
So 1350980-14-1 is a valid CAS Registry Number.
1350980-14-1Relevant articles and documents
Catalytic enantioselective iodoetherification of oximes
Tripathi, Chandra Bhushan,Mukherjee, Santanu
, p. 8450 - 8453 (2013)
Organocatalysis: The first catalytic enantioselective iodoetherification of oximes is developed using commercially available N-iodosuccinimide. In the presence of a dihydrocinchonidine-derived thiourea (10 mol %), β,γ-unsaturated oximes undergo facile iodoetherification to produce Δ2-isoxazolines containing a quaternary stereogenic center generally in high yield with good to excellent enantioselectivity. Copyright
